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Volumn 23, Issue 1-2, 2012, Pages 28-39

Canine epilepsy genetics

Author keywords

[No Author keywords available]

Indexed keywords

ABSENCE; ANIMAL GENETICS; ARTICLE; BREEDING; CLINICAL FEATURE; DOG; ELECTROENCEPHALOGRAPHY; EPILEPSY; GENE FUNCTION; GENE MUTATION; GENETIC ASSOCIATION; GENETIC MODEL; HUMAN; IDIOPATHIC EPILEPSY; MISSENSE MUTATION; MYOCLONUS EPILEPSY; NONHUMAN; PEDIGREE ANALYSIS; PHENOTYPE;

EID: 84857371891     PISSN: 09388990     EISSN: 14321777     Source Type: Journal    
DOI: 10.1007/s00335-011-9362-2     Document Type: Article
Times cited : (30)

References (108)
  • 1
    • 77957069126 scopus 로고    scopus 로고
    • A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis
    • 20679209 1:CAS:528:DC%2BC3cXhtVKqtrfL 10.1073/pnas.0914206107
    • M Abitbol JL Thibaud NJ Olby C Hitte JP Puech, et al. 2010 A canine Arylsulfatase G (ARSG) mutation leading to a sulfatase deficiency is associated with neuronal ceroid lipofuscinosis Proc Natl Acad Sci USA 107 14775 14780 20679209 1:CAS:528:DC%2BC3cXhtVKqtrfL 10.1073/pnas.0914206107
    • (2010) Proc Natl Acad Sci USA , vol.107 , pp. 14775-14780
    • Abitbol, M.1    Thibaud, J.L.2    Olby, N.J.3    Hitte, C.4    Puech, J.P.5
  • 2
    • 79955521023 scopus 로고    scopus 로고
    • Polymorphisms in the ABCB1 gene in phenobarbital responsive and resistant idiopathic epileptic Border Collies
    • 21488961 1:STN:280:DC%2BC3MvotFClsg%3D%3D 10.1111/j.1939-1676.2011.0718.x
    • L Alves V Hulsmeyer A Jaggy A Fischer T Leeb, et al. 2011 Polymorphisms in the ABCB1 gene in phenobarbital responsive and resistant idiopathic epileptic Border Collies J Vet Intern Med 25 484 489 21488961 1:STN:280: DC%2BC3MvotFClsg%3D%3D 10.1111/j.1939-1676.2011.0718.x
    • (2011) J Vet Intern Med , vol.25 , pp. 484-489
    • Alves, L.1    Hulsmeyer, V.2    Jaggy, A.3    Fischer, A.4    Leeb, T.5
  • 3
    • 33748966447 scopus 로고    scopus 로고
    • A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis
    • 16621647 1:CAS:528:DC%2BD28XhtVajsL7N 10.1016/j.ymgme.2006.02.016
    • T Awano ML Katz DP O'Brien I Sohar P Lobel, et al. 2006 A frame shift mutation in canine TPP1 (the ortholog of human CLN2) in a juvenile Dachshund with neuronal ceroid lipofuscinosis Mol Genet Metab 89 254 260 16621647 1:CAS:528:DC%2BD28XhtVajsL7N 10.1016/j.ymgme.2006.02.016
    • (2006) Mol Genet Metab , vol.89 , pp. 254-260
    • Awano, T.1    Katz, M.L.2    O'Brien, D.P.3    Sohar, I.4    Lobel, P.5
  • 4
    • 33645130942 scopus 로고    scopus 로고
    • A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis
    • 16386934 1:CAS:528:DC%2BD28XivVGrtb4%3D 10.1016/j.ymgme.2005.11.005
    • T Awano ML Katz DP O'Brien JF Taylor J Evans, et al. 2006 A mutation in the cathepsin D gene (CTSD) in American Bulldogs with neuronal ceroid lipofuscinosis Mol Genet Metab 87 341 348 16386934 1:CAS:528: DC%2BD28XivVGrtb4%3D 10.1016/j.ymgme.2005.11.005
    • (2006) Mol Genet Metab , vol.87 , pp. 341-348
    • Awano, T.1    Katz, M.L.2    O'Brien, D.P.3    Taylor, J.F.4    Evans, J.5
  • 5
    • 70350385236 scopus 로고    scopus 로고
    • Advances on the genetics of Mendelian idiopathic epilepsies
    • 19853223 10.1016/j.ncl.2009.07.001
    • S Baulac M Baulac 2009 Advances on the genetics of Mendelian idiopathic epilepsies Neurol Clin 27 1041 1061 19853223 10.1016/j.ncl.2009.07.001
    • (2009) Neurol Clin , vol.27 , pp. 1041-1061
    • Baulac, S.1    Baulac, M.2
  • 6
    • 34447569298 scopus 로고    scopus 로고
    • Copy number variants and genetic traits: Closer to the resolution of phenotypic to genotypic variability
    • 17637735 1:CAS:528:DC%2BD2sXnvVekt7k%3D 10.1038/nrg2149
    • JS Beckmann X Estivill SE Antonarakis 2007 Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability Nat Rev Genet 8 639 646 17637735 1:CAS:528:DC%2BD2sXnvVekt7k%3D 10.1038/nrg2149
    • (2007) Nat Rev Genet , vol.8 , pp. 639-646
    • Beckmann, J.S.1    Estivill, X.2    Antonarakis, S.E.3
  • 7
    • 0032930476 scopus 로고    scopus 로고
    • Electroencephalography in dogs with epilepsy: Similarities between human and canine findings
    • 10348156 1:STN:280:DyaK1M3nsF2isA%3D%3D 10.1111/j.1600-0404.1999.tb00676. x
    • M Berendt H Hogenhaven A Flagstad M Dam 1999 Electroencephalography in dogs with epilepsy: similarities between human and canine findings Acta Neurol Scand 99 276 283 10348156 1:STN:280:DyaK1M3nsF2isA%3D%3D 10.1111/j.1600-0404. 1999.tb00676.x
    • (1999) Acta Neurol Scand , vol.99 , pp. 276-283
    • Berendt, M.1    Hogenhaven, H.2    Flagstad, A.3    Dam, M.4
  • 8
    • 0036583465 scopus 로고    scopus 로고
    • A cross-sectional study of epilepsy in Danish Labrador Retrievers: Prevalence and selected risk factors
    • 12041655 10.1111/j.1939-1676.2002.tb02367.x
    • M Berendt H Gredal LG Pedersen L Alban J Alving 2002 A cross-sectional study of epilepsy in Danish Labrador Retrievers: prevalence and selected risk factors J Vet Intern Med 16 262 268 12041655 10.1111/j.1939-1676.2002.tb02367.x
    • (2002) J Vet Intern Med , vol.16 , pp. 262-268
    • Berendt, M.1    Gredal, H.2    Pedersen, L.G.3    Alban, L.4    Alving, J.5
  • 9
    • 59149087550 scopus 로고    scopus 로고
    • Prevalence and characteristics of epilepsy in the Belgian shepherd variants Groenendael and Tervueren born in Denmark 1995-2004
    • 19102738 10.1186/1751-0147-50-51
    • M Berendt CH Gullov SLK Christensen H Gudmundsdottir H Gredal, et al. 2008 Prevalence and characteristics of epilepsy in the Belgian shepherd variants Groenendael and Tervueren born in Denmark 1995-2004 Acta Vet Scand 50 51 19102738 10.1186/1751-0147-50-51
    • (2008) Acta Vet Scand , vol.50 , pp. 51
    • Berendt, M.1    Gullov, C.H.2    Christensen, S.L.K.3    Gudmundsdottir, H.4    Gredal, H.5
  • 10
    • 71149111174 scopus 로고    scopus 로고
    • Focal epilepsy in the Belgian shepherd: Evidence for simple Mendelian inheritance
    • 19954442 1:STN:280:DC%2BD1Mjpslyruw%3D%3D 10.1111/j.1748-5827.2009.00849. x
    • M Berendt CH Gullov M Fredholm 2009 Focal epilepsy in the Belgian shepherd: evidence for simple Mendelian inheritance J Small Anim Pract 50 655 661 19954442 1:STN:280:DC%2BD1Mjpslyruw%3D%3D 10.1111/j.1748-5827.2009.00849.x
    • (2009) J Small Anim Pract , vol.50 , pp. 655-661
    • Berendt, M.1    Gullov, C.H.2    Fredholm, M.3
  • 11
    • 77950857874 scopus 로고    scopus 로고
    • Revised terminology and concepts for organization of seizures and epilepsies: Report of the ILAE Commission on Classification and Terminology, 2005-2009
    • 20196795 10.1111/j.1528-1167.2010.02522.x
    • AT Berg SF Berkovic MJ Brodie J Buchhalter JH Cross, et al. 2010 Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009 Epilepsia 51 676 685 20196795 10.1111/j.1528-1167.2010.02522.x
    • (2010) Epilepsia , vol.51 , pp. 676-685
    • Berg, A.T.1    Berkovic, S.F.2    Brodie, M.J.3    Buchhalter, J.4    Cross, J.H.5
  • 12
    • 0015185107 scopus 로고
    • Sire- and sex-related differences in rates of epileptiform seizures in a purebred beagle dog colony
    • 5131425 1:STN:280:DyaE38%2FntlCisg%3D%3D
    • SW Bielfelt HC Redman RO McClellan 1971 Sire- and sex-related differences in rates of epileptiform seizures in a purebred beagle dog colony Am J Vet Res 32 2039 2048 5131425 1:STN:280:DyaE38%2FntlCisg%3D%3D
    • (1971) Am J Vet Res , vol.32 , pp. 2039-2048
    • Bielfelt, S.W.1    Redman, H.C.2    McClellan, R.O.3
  • 13
    • 77957372574 scopus 로고    scopus 로고
    • A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice
    • 10.1371/journal.pgen.1001046 1:CAS:528:DC%2BC3cXhtVWmsb7M
    • RM Boumil VA Letts MC Roberts C Lenz CL Mahaffey, et al. 2010 A missense mutation in a highly conserved alternate exon of dynamin-1 causes epilepsy in fitful mice PLoS Genet 6 e1001046 10.1371/journal.pgen.1001046 1:CAS:528:DC%2BC3cXhtVWmsb7M
    • (2010) PLoS Genet , vol.6 , pp. 1001046
    • Boumil, R.M.1    Letts, V.A.2    Roberts, M.C.3    Lenz, C.4    Mahaffey, C.L.5
  • 15
    • 0141618459 scopus 로고    scopus 로고
    • Mutations in NHLRC1 cause progressive myoclonus epilepsy
    • 12958597 1:CAS:528:DC%2BD3sXns1Wgt7Y%3D 10.1038/ng1238
    • EM Chan EJ Young L Ianzano I Munteanu X Zhao, et al. 2003 Mutations in NHLRC1 cause progressive myoclonus epilepsy Nat Genet 35 125 127 12958597 1:CAS:528:DC%2BD3sXns1Wgt7Y%3D 10.1038/ng1238
    • (2003) Nat Genet , vol.35 , pp. 125-127
    • Chan, E.M.1    Young, E.J.2    Ianzano, L.3    Munteanu, I.4    Zhao, X.5
  • 16
    • 61849154119 scopus 로고    scopus 로고
    • Mapping DNA structural variation in dogs
    • 19015322 1:CAS:528:DC%2BD1MXjt12kurc%3D 10.1101/gr.083741.108
    • WK Chen JD Swartz LJ Rush CE Alvarez 2009 Mapping DNA structural variation in dogs Genome Res 19 500 509 19015322 1:CAS:528:DC%2BD1MXjt12kurc%3D 10.1101/gr.083741.108
    • (2009) Genome Res , vol.19 , pp. 500-509
    • Chen, W.K.1    Swartz, J.D.2    Rush, L.J.3    Alvarez, C.E.4
  • 17
    • 74249088463 scopus 로고    scopus 로고
    • Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies
    • 19843651 10.1093/brain/awp262
    • CG de Kovel H Trucks I Helbig HC Mefford C Baker, et al. 2010 Recurrent microdeletions at 15q11.2 and 16p13.11 predispose to idiopathic generalized epilepsies Brain 133 23 32 19843651 10.1093/brain/awp262
    • (2010) Brain , vol.133 , pp. 23-32
    • De Kovel, C.G.1    Trucks, H.2    Helbig, I.3    Mefford, H.C.4    Baker, C.5
  • 18
    • 70350774172 scopus 로고    scopus 로고
    • Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: Precedent for disorders with complex inheritance
    • 19592580 1:CAS:528:DC%2BD1MXhtFagsbjL 10.1093/hmg/ddp311
    • LM Dibbens S Mullen I Helbig HC Mefford MA Bayly, et al. 2009 Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance Hum Mol Genet 18 3626 3631 19592580 1:CAS:528:DC%2BD1MXhtFagsbjL 10.1093/hmg/ddp311
    • (2009) Hum Mol Genet , vol.18 , pp. 3626-3631
    • Dibbens, L.M.1    Mullen, S.2    Helbig, I.3    Mefford, H.C.4    Bayly, M.A.5
  • 20
    • 79954991060 scopus 로고    scopus 로고
    • Candidate genes for idiopathic epilepsy in four dog breeds
    • 21518446 10.1186/1471-2156-12-38
    • KJ Ekenstedt EE Patterson KM Minor JR Mickelson 2011 Candidate genes for idiopathic epilepsy in four dog breeds BMC Genet 12 38 21518446 10.1186/1471-2156-12-38
    • (2011) BMC Genet , vol.12 , pp. 38
    • Ekenstedt, K.J.1    Patterson, E.E.2    Minor, K.M.3    Mickelson, J.R.4
  • 21
    • 0033797135 scopus 로고    scopus 로고
    • Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability
    • 11026449 1:CAS:528:DC%2BD3cXnsFChsrw%3D 10.1002/1531-8249(200010)48: 4<647::AID-ANA12>3.0.CO;2-Q
    • LH Eunson R Rea SM Zuberi S Youroukos CP Panayiotopoulos, et al. 2000 Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability Ann Neurol 48 647 656 11026449 1:CAS:528:DC%2BD3cXnsFChsrw%3D 10.1002/1531-8249(200010)48:4<647::AID- ANA12>3.0.CO;2-Q
    • (2000) Ann Neurol , vol.48 , pp. 647-656
    • Eunson, L.H.1    Rea, R.2    Zuberi, S.M.3    Youroukos, S.4    Panayiotopoulos, C.P.5
  • 22
    • 13544272793 scopus 로고    scopus 로고
    • A variant form of neuronal ceroid lipofuscinosis in American bulldogs
    • 15715047 10.1111/j.1939-1676.2005.tb02657.x
    • J Evans ML Katz D Levesque GD Shelton A de Lahunta, et al. 2005 A variant form of neuronal ceroid lipofuscinosis in American bulldogs J Vet Intern Med 19 44 51 15715047 10.1111/j.1939-1676.2005.tb02657.x
    • (2005) J Vet Intern Med , vol.19 , pp. 44-51
    • Evans, J.1    Katz, M.L.2    Levesque, D.3    Shelton, G.D.4    De Lahunta, A.5
  • 23
    • 0016267210 scopus 로고
    • The genetics of epilepsy in the British Alsatian
    • 4449202 1:STN:280:DyaE2M%2FpvVyktw%3D%3D 10.1111/j.1748-5827.1974. tb05651.x
    • MJ Falco J Barker ME Wallace 1974 The genetics of epilepsy in the British Alsatian J Small Anim Pract 15 685 692 4449202 1:STN:280:DyaE2M%2FpvVyktw%3D%3D 10.1111/j.1748-5827.1974.tb05651.x
    • (1974) J Small Anim Pract , vol.15 , pp. 685-692
    • Falco, M.J.1    Barker, J.2    Wallace, M.E.3
  • 24
    • 0034686843 scopus 로고    scopus 로고
    • Segregation analysis of epilepsy in the Belgian tervueren dog
    • 10994924 1:STN:280:DC%2BD3cvksVGmsg%3D%3D 10.1136/vr.147.8.218
    • TR Famula AM Oberbauer 2000 Segregation analysis of epilepsy in the Belgian tervueren dog Vet Rec 147 218 221 10994924 1:STN:280: DC%2BD3cvksVGmsg%3D%3D 10.1136/vr.147.8.218
    • (2000) Vet Rec , vol.147 , pp. 218-221
    • Famula, T.R.1    Oberbauer, A.M.2
  • 25
    • 0031201193 scopus 로고    scopus 로고
    • Heritability of epileptic seizures in the Belgian tervueren
    • 9282341 1:STN:280:DyaK2svislejuw%3D%3D 10.1111/j.1748-5827.1997.tb03483.x
    • TR Famula AM Oberbauer KN Brown 1997 Heritability of epileptic seizures in the Belgian tervueren J Small Anim Pract 38 349 352 9282341 1:STN:280:DyaK2svislejuw%3D%3D 10.1111/j.1748-5827.1997.tb03483.x
    • (1997) J Small Anim Pract , vol.38 , pp. 349-352
    • Famula, T.R.1    Oberbauer, A.M.2    Brown, K.N.3
  • 26
    • 79954629520 scopus 로고    scopus 로고
    • A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers
    • 21362476 1:CAS:528:DC%2BC3MXkvVGksr0%3D 10.1016/j.nbd.2011.02.009
    • FH Farias R Zeng GS Johnson FA Wininger JF Taylor, et al. 2011 A truncating mutation in ATP13A2 is responsible for adult-onset neuronal ceroid lipofuscinosis in Tibetan terriers Neurobiol Dis 42 468 474 21362476 1:CAS:528:DC%2BC3MXkvVGksr0%3D 10.1016/j.nbd.2011.02.009
    • (2011) Neurobiol Dis , vol.42 , pp. 468-474
    • Farias, F.H.1    Zeng, R.2    Johnson, G.S.3    Wininger, F.A.4    Taylor, J.F.5
  • 27
    • 16344387731 scopus 로고    scopus 로고
    • Epileptic seizures and epilepsy: Definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE)
    • 15816939 10.1111/j.0013-9580.2005.66104.x
    • RS Fisher W van Emde Boas W Blume C Elger P Genton, et al. 2005 Epileptic seizures and epilepsy: definitions proposed by the International League Against Epilepsy (ILAE) and the International Bureau for Epilepsy (IBE) Epilepsia 46 470 472 15816939 10.1111/j.0013-9580.2005.66104.x
    • (2005) Epilepsia , vol.46 , pp. 470-472
    • Fisher, R.S.1    Van Emde Boas, W.2    Blume, W.3    Elger, C.4    Genton, P.5
  • 28
    • 0028021849 scopus 로고
    • Enhanced aspartate release related to epilepsy in (EL) mice
    • 7913488 1:CAS:528:DyaK2cXltVGqtr0%3D 10.1046/j.1471-4159.1994.63020592.x
    • HJ Flavin TN Seyfried 1994 Enhanced aspartate release related to epilepsy in (EL) mice J Neurochem 63 592 595 7913488 1:CAS:528:DyaK2cXltVGqtr0%3D 10.1046/j.1471-4159.1994.63020592.x
    • (1994) J Neurochem , vol.63 , pp. 592-595
    • Flavin, H.J.1    Seyfried, T.N.2
  • 29
    • 0030584085 scopus 로고    scopus 로고
    • Absence epilepsy in tottering mutant mice is associated with calcium channel defects
    • 8929530 1:CAS:528:DyaK28XntVars74%3D 10.1016/S0092-8674(00)81381-1
    • CF Fletcher CM Lutz TN O'Sullivan JD Shaughnessy Jr R Hawkes, et al. 1996 Absence epilepsy in tottering mutant mice is associated with calcium channel defects Cell 87 607 617 8929530 1:CAS:528:DyaK28XntVars74%3D 10.1016/S0092-8674(00)81381-1
    • (1996) Cell , vol.87 , pp. 607-617
    • Fletcher, C.F.1    Lutz, C.M.2    O'Sullivan, T.N.3    Shaughnessy Jr., J.D.4    Hawkes, R.5
  • 30
    • 0032860274 scopus 로고    scopus 로고
    • Detecting genes in new and old mouse models for epilepsy: A prospectus through the magnifying glass
    • 10515158 1:CAS:528:DyaK1MXlvVWrsLc%3D 10.1016/S0920-1211(99)00044-3
    • WN Frankel 1999 Detecting genes in new and old mouse models for epilepsy: a prospectus through the magnifying glass Epilepsy Res 36 97 110 10515158 1:CAS:528:DyaK1MXlvVWrsLc%3D 10.1016/S0920-1211(99)00044-3
    • (1999) Epilepsy Res , vol.36 , pp. 97-110
    • Frankel, W.N.1
  • 31
    • 0029443328 scopus 로고
    • Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci
    • 8747921 1:CAS:528:DyaK28Xos1aqsQ%3D%3D 10.1007/BF00292432
    • WN Frankel EW Johnson CM Lutz 1995 Congenic strains reveal effects of the epilepsy quantitative trait locus, El2, separate from other El loci Mamm Genome 6 839 843 8747921 1:CAS:528:DyaK28Xos1aqsQ%3D%3D 10.1007/BF00292432
    • (1995) Mamm Genome , vol.6 , pp. 839-843
    • Frankel, W.N.1    Johnson, E.W.2    Lutz, C.M.3
  • 32
    • 0029450469 scopus 로고
    • New seizure frequency QTL and the complex genetics of epilepsy in EL mice
    • 8747920 1:CAS:528:DyaK28Xos1aqsA%3D%3D 10.1007/BF00292431
    • WN Frankel A Valenzuela CM Lutz EW Johnson WF Dietrich, et al. 1995 New seizure frequency QTL and the complex genetics of epilepsy in EL mice Mamm Genome 6 830 838 8747920 1:CAS:528:DyaK28Xos1aqsA%3D%3D 10.1007/BF00292431
    • (1995) Mamm Genome , vol.6 , pp. 830-838
    • Frankel, W.N.1    Valenzuela, A.2    Lutz, C.M.3    Johnson, E.W.4    Dietrich, W.F.5
  • 33
    • 32944459586 scopus 로고    scopus 로고
    • Genetics of idiopathic generalized epilepsies
    • 16302872 1:CAS:528:DC%2BD2MXhtlamsrnM 10.1111/j.1528-1167.2005.00310.x
    • M Gardiner 2005 Genetics of idiopathic generalized epilepsies Epilepsia 46 Suppl 9 15 20 16302872 1:CAS:528:DC%2BD2MXhtlamsrnM 10.1111/j.1528-1167.2005. 00310.x
    • (2005) Epilepsia , vol.46 , Issue.SUPPL. 9 , pp. 15-20
    • Gardiner, M.1
  • 34
    • 15244352202 scopus 로고    scopus 로고
    • Lafora disease due to EPM2B mutations: A clinical and genetic study
    • 15781812 1:CAS:528:DC%2BD2MXhvVShsL4%3D 10.1212/01.WNL.0000154519.10805. F7
    • C Gomez-Abad P Gomez-Garre E Gutierrez-Delicado S Saygi R Michelucci, et al. 2005 Lafora disease due to EPM2B mutations: a clinical and genetic study Neurology 64 982 986 15781812 1:CAS:528:DC%2BD2MXhvVShsL4%3D 10.1212/01.WNL.0000154519.10805.F7
    • (2005) Neurology , vol.64 , pp. 982-986
    • Gomez-Abad, C.1    Gomez-Garre, P.2    Gutierrez-Delicado, E.3    Saygi, S.4    Michelucci, R.5
  • 35
    • 34547105807 scopus 로고    scopus 로고
    • The state of the art in the genetic analysis of the epilepsies
    • 17618539 1:CAS:528:DC%2BD2sXptFGqtLk%3D 10.1007/s11910-007-0049-8
    • DA Greenberg DK Pal 2007 The state of the art in the genetic analysis of the epilepsies Curr Neurol Neurosci Rep 7 320 328 17618539 1:CAS:528: DC%2BD2sXptFGqtLk%3D 10.1007/s11910-007-0049-8
    • (2007) Curr Neurol Neurosci Rep , vol.7 , pp. 320-328
    • Greenberg, D.A.1    Pal, D.K.2
  • 36
    • 33947229268 scopus 로고    scopus 로고
    • New ideas in epilepsy genetics: Novel epilepsy genes, copy number alterations, and gene regulation
    • 17353374 10.1001/archneur.64.3.324
    • CA Gurnett P Hedera 2007 New ideas in epilepsy genetics: novel epilepsy genes, copy number alterations, and gene regulation Arch Neurol 64 324 328 17353374 10.1001/archneur.64.3.324
    • (2007) Arch Neurol , vol.64 , pp. 324-328
    • Gurnett, C.A.1    Hedera, P.2
  • 37
    • 0029917067 scopus 로고    scopus 로고
    • Canine epilepsy: A genetic counseling programme for keeshonds
    • 8737262 1:STN:280:DyaK283pvVWrug%3D%3D 10.1136/vr.138.15.358
    • SJ Hall ME Wallace 1996 Canine epilepsy: a genetic counseling programme for keeshonds Vet Rec 138 358 360 8737262 1:STN:280:DyaK283pvVWrug%3D%3D 10.1136/vr.138.15.358
    • (1996) Vet Rec , vol.138 , pp. 358-360
    • Hall, S.J.1    Wallace, M.E.2
  • 38
    • 0004452545 scopus 로고
    • Progressive familial myoclonic epilepsy in three families: Its clinical features and pathological basis
    • 13269595 1:CAS:528:DyaG28XhtlCjsA%3D%3D 10.1093/brain/78.3.325
    • DG Harriman JH Millar AC Stevenson 1955 Progressive familial myoclonic epilepsy in three families: its clinical features and pathological basis Brain 78 325 349 13269595 1:CAS:528:DyaG28XhtlCjsA%3D%3D 10.1093/brain/78.3.325
    • (1955) Brain , vol.78 , pp. 325-349
    • Harriman, D.G.1    Millar, J.H.2    Stevenson, A.C.3
  • 39
    • 77952096810 scopus 로고    scopus 로고
    • Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes
    • 20398883 1:CAS:528:DC%2BC3cXms1arsLY%3D 10.1016/j.ajhg.2010.03.018
    • EL Heinzen RA Radtke TJ Urban GL Cavalleri C Depondt, et al. 2010 Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes Am J Hum Genet 86 707 718 20398883 1:CAS:528:DC%2BC3cXms1arsLY%3D 10.1016/j.ajhg.2010.03.018
    • (2010) Am J Hum Genet , vol.86 , pp. 707-718
    • Heinzen, E.L.1    Radtke, R.A.2    Urban, T.J.3    Cavalleri, G.L.4    Depondt, C.5
  • 40
    • 59149096726 scopus 로고    scopus 로고
    • 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy
    • 19136953 1:CAS:528:DC%2BD1MXktVehsg%3D%3D 10.1038/ng.292
    • I Helbig HC Mefford AJ Sharp M Guipponi M Fichera, et al. 2009 15q13.3 microdeletions increase risk of idiopathic generalized epilepsy Nat Genet 41 160 162 19136953 1:CAS:528:DC%2BD1MXktVehsg%3D%3D 10.1038/ng.292
    • (2009) Nat Genet , vol.41 , pp. 160-162
    • Helbig, I.1    Mefford, H.C.2    Sharp, A.J.3    Guipponi, M.4    Fichera, M.5
  • 41
    • 73349083097 scopus 로고    scopus 로고
    • Epilepsy in Border Collies: Clinical manifestation, outcome, and mode of inheritance
    • 20391637 1:STN:280:DC%2BC3c3mtFOmtQ%3D%3D 10.1111/j.1939-1676.2009.0438.x
    • V Hulsmeyer R Zimmermann C Brauer C Sauter-Louis A Fischer 2010 Epilepsy in Border Collies: clinical manifestation, outcome, and mode of inheritance J Vet Intern Med 24 171 178 20391637 1:STN:280:DC%2BC3c3mtFOmtQ%3D%3D 10.1111/j.1939-1676.2009.0438.x
    • (2010) J Vet Intern Med , vol.24 , pp. 171-178
    • Hulsmeyer, V.1    Zimmermann, R.2    Brauer, C.3    Sauter-Louis, C.4    Fischer, A.5
  • 42
    • 10344235279 scopus 로고    scopus 로고
    • Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia
    • 15483044 10.1093/brain/awh301
    • P Imbrici SL Jaffe LH Eunson NP Davies C Herd, et al. 2004 Dysfunction of the brain calcium channel CaV2.1 in absence epilepsy and episodic ataxia Brain 127 2682 2692 15483044 10.1093/brain/awh301
    • (2004) Brain , vol.127 , pp. 2682-2692
    • Imbrici, P.1    Jaffe, S.L.2    Eunson, L.H.3    Davies, N.P.4    Herd, C.5
  • 43
    • 0032085761 scopus 로고    scopus 로고
    • Genetic aspects of idiopathic epilepsy in Labrador retrievers
    • 9673903 1:STN:280:DyaK1czjvVKqsw%3D%3D 10.1111/j.1748-5827.1998.tb03650.x
    • A Jaggy D Faissler C Gaillard P Srenk H Graber 1998 Genetic aspects of idiopathic epilepsy in Labrador retrievers J Small Anim Pract 39 275 280 9673903 1:STN:280:DyaK1czjvVKqsw%3D%3D 10.1111/j.1748-5827.1998.tb03650.x
    • (1998) J Small Anim Pract , vol.39 , pp. 275-280
    • Jaggy, A.1    Faissler, D.2    Gaillard, C.3    Srenk, P.4    Graber, H.5
  • 44
    • 62949195147 scopus 로고    scopus 로고
    • Neuronal ceroid lipofuscinoses
    • 19084560 1:CAS:528:DC%2BD1MXjslOlsbY%3D 10.1016/j.bbamcr.2008.11.004
    • A Jalanko T Braulke 2009 Neuronal ceroid lipofuscinoses Biochim Biophys Acta 1793 697 709 19084560 1:CAS:528:DC%2BD1MXjslOlsbY%3D 10.1016/j.bbamcr.2008. 11.004
    • (2009) Biochim Biophys Acta , vol.1793 , pp. 697-709
    • Jalanko, A.1    Braulke, T.2
  • 45
    • 32944457671 scopus 로고    scopus 로고
    • Epidemiology of idiopathic generalized epilepsies
    • 16302871 10.1111/j.1528-1167.2005.00309.x
    • P Jallon P Latour 2005 Epidemiology of idiopathic generalized epilepsies Epilepsia 46 Suppl 9 10 14 16302871 10.1111/j.1528-1167.2005.00309.x
    • (2005) Epilepsia , vol.46 , Issue.SUPPL. 9 , pp. 10-14
    • Jallon, P.1    Latour, P.2
  • 46
    • 37349015922 scopus 로고    scopus 로고
    • Electroencephalography findings in healthy and Finnish Spitz dogs with epilepsy: Visual and background quantitative analysis
    • 18196740 10.1111/j.1939-1676.2007.tb01952.x
    • J Jeserevics R Viitmaa S Cizinauskas K Sainio TS Jokinen, et al. 2007 Electroencephalography findings in healthy and Finnish Spitz dogs with epilepsy: visual and background quantitative analysis J Vet Intern Med 21 1299 1306 18196740 10.1111/j.1939-1676.2007.tb01952.x
    • (2007) J Vet Intern Med , vol.21 , pp. 1299-1306
    • Jeserevics, J.1    Viitmaa, R.2    Cizinauskas, S.3    Sainio, K.4    Jokinen, T.S.5
  • 47
    • 34249279792 scopus 로고    scopus 로고
    • Benign familial juvenile epilepsy in Lagotto Romagnolo dogs
    • 17552452 1:STN:280:DC%2BD2szktVGjsQ%3D%3D 10.1111/j.1939-1676.2007. tb02991.x
    • TS Jokinen L Metsahonkala L Bergamasco R Viitmaa P Syrja, et al. 2007 Benign familial juvenile epilepsy in Lagotto Romagnolo dogs J Vet Intern Med 21 464 471 17552452 1:STN:280:DC%2BD2szktVGjsQ%3D%3D 10.1111/j.1939-1676.2007. tb02991.x
    • (2007) J Vet Intern Med , vol.21 , pp. 464-471
    • Jokinen, T.S.1    Metsahonkala, L.2    Bergamasco, L.3    Viitmaa, R.4    Syrja, P.5
  • 48
    • 0035828406 scopus 로고    scopus 로고
    • Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel
    • 11564488 1:CAS:528:DC%2BD3MXmvVKmsbs%3D 10.1016/S0140-6736(01)05971-2
    • A Jouvenceau LH Eunson A Spauschus V Ramesh SM Zuberi, et al. 2001 Human epilepsy associated with dysfunction of the brain P/Q-type calcium channel Lancet 358 801 807 11564488 1:CAS:528:DC%2BD3MXmvVKmsbs%3D 10.1016/S0140- 6736(01)05971-2
    • (2001) Lancet , vol.358 , pp. 801-807
    • Jouvenceau, A.1    Eunson, L.H.2    Spauschus, A.3    Ramesh, V.4    Zuberi, S.M.5
  • 49
    • 0033159433 scopus 로고    scopus 로고
    • Clinical and genetic investigations of idiopathic epilepsy in the Bernese mountain dog
    • 10444751 1:STN:280:DyaK1MzntlOktQ%3D%3D 10.1111/j.1748-5827.1999.tb03089. x
    • I Kathmann A Jaggy A Busato M Bartschi C Gaillard 1999 Clinical and genetic investigations of idiopathic epilepsy in the Bernese mountain dog J Small Anim Pract 40 319 325 10444751 1:STN:280:DyaK1MzntlOktQ%3D%3D 10.1111/j.1748-5827.1999.tb03089.x
    • (1999) J Small Anim Pract , vol.40 , pp. 319-325
    • Kathmann, I.1    Jaggy, A.2    Busato, A.3    Bartschi, M.4    Gaillard, C.5
  • 50
    • 11144341883 scopus 로고    scopus 로고
    • A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis
    • 15629147 1:CAS:528:DC%2BD2MXksF2q 10.1016/j.bbrc.2004.12.038
    • ML Katz S Khan T Awano SA Shahid AN Siakotos, et al. 2005 A mutation in the CLN8 gene in English Setter dogs with neuronal ceroid-lipofuscinosis Biochem Biophys Res Commun 327 541 547 15629147 1:CAS:528:DC%2BD2MXksF2q 10.1016/j.bbrc.2004.12.038
    • (2005) Biochem Biophys Res Commun , vol.327 , pp. 541-547
    • Katz, M.L.1    Khan, S.2    Awano, T.3    Shahid, S.A.4    Siakotos, A.N.5
  • 51
    • 79952231932 scopus 로고    scopus 로고
    • A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis
    • 21234413 10.1155/2011/198042 1:CAS:528:DC%2BC3MXjvVWrsQ%3D%3D
    • ML Katz FH Farias DN Sanders R Zeng S Khan, et al. 2011 A missense mutation in canine CLN6 in an Australian shepherd with neuronal ceroid lipofuscinosis J Biomed Biotechnol 2011 198042 21234413 10.1155/2011/198042 1:CAS:528:DC%2BC3MXjvVWrsQ%3D%3D
    • (2011) J Biomed Biotechnol , vol.2011 , pp. 198042
    • Katz, M.L.1    Farias, F.H.2    Sanders, D.N.3    Zeng, R.4    Khan, S.5
  • 52
    • 73949160744 scopus 로고    scopus 로고
    • Pharmacogenetic association study of 30 genes with phenobarbital drug response in epileptic dogs
    • 1:CAS:528:DC%2BD1MXhsVeku7fI 10.1097/FPC.0b013e3283307cba
    • EM Kennerly Y Idaghdour NJ Olby KR Munana G Gibson 2009 Pharmacogenetic association study of 30 genes with phenobarbital drug response in epileptic dogs Pharmacogenet Genomics 19 12 911 922 1:CAS:528:DC%2BD1MXhsVeku7fI 10.1097/FPC.0b013e3283307cba
    • (2009) Pharmacogenet Genomics , vol.19 , Issue.12 , pp. 911-922
    • Kennerly, E.M.1    Idaghdour, Y.2    Olby, N.J.3    Munana, K.R.4    Gibson, G.5
  • 53
    • 0033975420 scopus 로고    scopus 로고
    • A major effect QTL determined by multiple genes in epileptic EL mice
    • 10645948 1:CAS:528:DC%2BD3cXpslyquw%3D%3D
    • ME Legare FS Bartlett II WN Frankel 2000 A major effect QTL determined by multiple genes in epileptic EL mice Genome Res 10 42 48 10645948 1:CAS:528:DC%2BD3cXpslyquw%3D%3D
    • (2000) Genome Res , vol.10 , pp. 42-48
    • Legare, M.E.1    Bartlett, I.I.F.S.2    Frankel, W.N.3
  • 54
    • 79961126069 scopus 로고    scopus 로고
    • LUPA: A European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs
    • 21752675 10.1016/j.tvjl.2011.06.013
    • AS Lequarre L Andersson C Andre M Fredholm C Hitte, et al. 2011 LUPA: A European initiative taking advantage of the canine genome architecture for unravelling complex disorders in both human and dogs Vet J 189 2 155 159 21752675 10.1016/j.tvjl.2011.06.013
    • (2011) Vet J , vol.189 , Issue.2 , pp. 155-159
    • Lequarre, A.S.1    Andersson, L.2    Andre, C.3    Fredholm, M.4    Hitte, C.5
  • 55
    • 0036816431 scopus 로고    scopus 로고
    • Clinical presentations of naturally occurring canine seizures: Similarities to human seizures
    • 12609269 10.1016/S1525-5050(02)00523-1
    • BG Licht MH Licht KM Harper S Lin JJ Curtin, et al. 2002 Clinical presentations of naturally occurring canine seizures: similarities to human seizures Epilepsy Behav 3 460 470 12609269 10.1016/S1525-5050(02)00523-1
    • (2002) Epilepsy Behav , vol.3 , pp. 460-470
    • Licht, B.G.1    Licht, M.H.2    Harper, K.M.3    Lin, S.4    Curtin, J.J.5
  • 56
    • 37349061352 scopus 로고    scopus 로고
    • Clinical characteristics and mode of inheritance of familial focal seizures in Standard Poodles
    • 18020993 10.2460/javma.231.10.1520
    • BG Licht S Lin Y Luo LL Hyson MH Licht, et al. 2007 Clinical characteristics and mode of inheritance of familial focal seizures in Standard Poodles J Am Vet Med Assoc 231 1520 1528 18020993 10.2460/javma.231.10.1520
    • (2007) J Am Vet Med Assoc , vol.231 , pp. 1520-1528
    • Licht, B.G.1    Lin, S.2    Luo, Y.3    Hyson, L.L.4    Licht, M.H.5
  • 57
    • 28644447707 scopus 로고    scopus 로고
    • Genome sequence, comparative analysis and haplotype structure of the domestic dog
    • 16341006 1:CAS:528:DC%2BD2MXht1yns7%2FF 10.1038/nature04338
    • K Lindblad-Toh CM Wade TS Mikkelsen EK Karlsson DB Jaffe, et al. 2005 Genome sequence, comparative analysis and haplotype structure of the domestic dog Nature 438 803 819 16341006 1:CAS:528:DC%2BD2MXht1yns7%2FF 10.1038/nature04338
    • (2005) Nature , vol.438 , pp. 803-819
    • Lindblad-Toh, K.1    Wade, C.M.2    Mikkelsen, T.S.3    Karlsson, E.K.4    Jaffe, D.B.5
  • 58
    • 19944429189 scopus 로고    scopus 로고
    • Expanded repeat in canine epilepsy
    • 15637270 1:CAS:528:DC%2BD2MXitlantA%3D%3D 10.1126/science.1102832
    • H Lohi EJ Young SN Fitzmaurice C Rusbridge EM Chan, et al. 2005 Expanded repeat in canine epilepsy Science 307 81 15637270 1:CAS:528: DC%2BD2MXitlantA%3D%3D 10.1126/science.1102832
    • (2005) Science , vol.307 , pp. 81
    • Lohi, H.1    Young, E.J.2    Fitzmaurice, S.N.3    Rusbridge, C.4    Chan, E.M.5
  • 60
    • 0343990077 scopus 로고    scopus 로고
    • Animal models of intractable epilepsy
    • 9364612 1:STN:280:DyaK1c%2FjtFWqtw%3D%3D 10.1016/S0301-0082(97)00035-X
    • W Loscher 1997 Animal models of intractable epilepsy Prog Neurobiol 53 239 258 9364612 1:STN:280:DyaK1c%2FjtFWqtw%3D%3D 10.1016/S0301-0082(97)00035-X
    • (1997) Prog Neurobiol , vol.53 , pp. 239-258
    • Loscher, W.1
  • 61
    • 0032568048 scopus 로고    scopus 로고
    • Epilepsy genetics: An abundance of riches for biologists
    • 9501059 1:CAS:528:DyaK1cXhvVWqt7o%3D 10.1016/S0960-9822(98)70102-2
    • JO McNamara RS Puranam 1998 Epilepsy genetics: an abundance of riches for biologists Curr Biol 8 R168 R170 9501059 1:CAS:528:DyaK1cXhvVWqt7o%3D 10.1016/S0960-9822(98)70102-2
    • (1998) Curr Biol , vol.8
    • McNamara, J.O.1    Puranam, R.S.2
  • 62
    • 77956628767 scopus 로고    scopus 로고
    • Genome-wide copy number variation in epilepsy: Novel susceptibility loci in idiopathic generalized and focal epilepsies
    • 20502679 10.1371/journal.pgen.1000962 1:CAS:528:DC%2BC3cXms1GgsbY%3D
    • HC Mefford H Muhle P Ostertag S von Spiczak K Buysse, et al. 2010 Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies PLoS Genet 6 e1000962 20502679 10.1371/journal.pgen.1000962 1:CAS:528:DC%2BC3cXms1GgsbY%3D
    • (2010) PLoS Genet , vol.6 , pp. 1000962
    • Mefford, H.C.1    Muhle, H.2    Ostertag, P.3    Von Spiczak, S.4    Buysse, K.5
  • 63
    • 0035676059 scopus 로고    scopus 로고
    • Identification of epilepsy genes in human and mouse
    • 11700294 1:CAS:528:DC%2BD38XlsVOm 10.1146/annurev.genet.35.102401.091142
    • MH Meisler J Kearney R Ottman A Escayg 2001 Identification of epilepsy genes in human and mouse Annu Rev Genet 35 567 588 11700294 1:CAS:528: DC%2BD38XlsVOm 10.1146/annurev.genet.35.102401.091142
    • (2001) Annu Rev Genet , vol.35 , pp. 567-588
    • Meisler, M.H.1    Kearney, J.2    Ottman, R.3    Escayg, A.4
  • 64
    • 23244466313 scopus 로고    scopus 로고
    • A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs
    • 16033706 1:CAS:528:DC%2BD2MXmvFCrtLw%3D 10.1016/j.ygeno.2005.06.005
    • SA Melville CL Wilson CS Chiang VP Studdert F Lingaas, et al. 2005 A mutation in canine CLN5 causes neuronal ceroid lipofuscinosis in Border collie dogs Genomics 86 287 294 16033706 1:CAS:528:DC%2BD2MXmvFCrtLw%3D 10.1016/j.ygeno.2005.06.005
    • (2005) Genomics , vol.86 , pp. 287-294
    • Melville, S.A.1    Wilson, C.L.2    Chiang, C.S.3    Studdert, V.P.4    Lingaas, F.5
  • 65
    • 17344362307 scopus 로고    scopus 로고
    • Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy
    • 9771710 1:CAS:528:DyaK1cXms1artbk%3D 10.1038/2470
    • BA Minassian JR Lee JA Herbrick J Huizenga S Soder, et al. 1998 Mutations in a gene encoding a novel protein tyrosine phosphatase cause progressive myoclonus epilepsy Nat Genet 20 171 174 9771710 1:CAS:528:DyaK1cXms1artbk%3D 10.1038/2470
    • (1998) Nat Genet , vol.20 , pp. 171-174
    • Minassian, B.A.1    Lee, J.R.2    Herbrick, J.A.3    Huizenga, J.4    Soder, S.5
  • 66
    • 0036181748 scopus 로고    scopus 로고
    • Cliniconeuropathologic findings of familial frontal lobe epilepsy in Shetland sheepdogs
    • 11858647 1:STN:280:DC%2BD387itlGjsA%3D%3D
    • T Morita A Shimada T Takeuchi Y Hikasa M Sawada, et al. 2002 Cliniconeuropathologic findings of familial frontal lobe epilepsy in Shetland sheepdogs Can J Vet Res 66 35 41 11858647 1:STN:280:DC%2BD387itlGjsA%3D%3D
    • (2002) Can J Vet Res , vol.66 , pp. 35-41
    • Morita, T.1    Shimada, A.2    Takeuchi, T.3    Hikasa, Y.4    Sawada, M.5
  • 67
    • 61849144443 scopus 로고    scopus 로고
    • The genomic architecture of segmental duplications and associated copy number variants in dogs
    • 19129542 1:CAS:528:DC%2BD1MXjt12kurY%3D 10.1101/gr.084715.108
    • TJ Nicholas Z Cheng M Ventura K Mealey EE Eichler, et al. 2009 The genomic architecture of segmental duplications and associated copy number variants in dogs Genome Res 19 491 499 19129542 1:CAS:528:DC%2BD1MXjt12kurY%3D 10.1101/gr.084715.108
    • (2009) Genome Res , vol.19 , pp. 491-499
    • Nicholas, T.J.1    Cheng, Z.2    Ventura, M.3    Mealey, K.4    Eichler, E.E.5
  • 68
    • 80051625199 scopus 로고    scopus 로고
    • A high-resolution integrated map of copy number polymorphisms within and between breeds of the modern domesticated dog
    • 21846351 10.1186/1471-2164-12-414
    • TJ Nicholas C Baker EE Eichler JM Akey 2011 A high-resolution integrated map of copy number polymorphisms within and between breeds of the modern domesticated dog BMC Genomics 12 414 21846351 10.1186/1471-2164-12-414
    • (2011) BMC Genomics , vol.12 , pp. 414
    • Nicholas, T.J.1    Baker, C.2    Eichler, E.E.3    Akey, J.M.4
  • 69
    • 0035432805 scopus 로고    scopus 로고
    • Heritability estimations for diseases, coat color, body weight, and height in a birth cohort of Boxers
    • 11497438 1:STN:280:DC%2BD3MvltFegtA%3D%3D 10.2460/ajvr.2001.62.1198
    • AL Nielen LL Janss BW Knol 2001 Heritability estimations for diseases, coat color, body weight, and height in a birth cohort of Boxers Am J Vet Res 62 1198 1206 11497438 1:STN:280:DC%2BD3MvltFegtA%3D%3D 10.2460/ajvr.2001.62.1198
    • (2001) Am J Vet Res , vol.62 , pp. 1198-1206
    • Nielen, A.L.1    Janss, L.L.2    Knol, B.W.3
  • 70
    • 63749094521 scopus 로고    scopus 로고
    • LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy
    • 19191227 1:CAS:528:DC%2BD1MXltFyiurg%3D 10.1002/humu.20925
    • C Nobile R Michelucci S Andreazza E Pasini SCE Tosatto 2009 LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy Hum Mutat 30 530 536 19191227 1:CAS:528:DC%2BD1MXltFyiurg%3D 10.1002/humu.20925
    • (2009) Hum Mutat , vol.30 , pp. 530-536
    • Nobile, C.1    Michelucci, R.2    Andreazza, S.3    Pasini, E.4    Tosatto, S.C.E.5
  • 71
    • 0346217094 scopus 로고    scopus 로고
    • The genetics of epilepsy in the Belgian tervuren and sheepdog
    • 12692163 1:CAS:528:DC%2BD3sXktVWhu7o%3D 10.1093/jhered/esg010
    • AM Oberbauer DI Grossman DN Irion AL Schaffer ML Eggleston, et al. 2003 The genetics of epilepsy in the Belgian tervuren and sheepdog J Hered 94 57 63 12692163 1:CAS:528:DC%2BD3sXktVWhu7o%3D 10.1093/jhered/esg010
    • (2003) J Hered , vol.94 , pp. 57-63
    • Oberbauer, A.M.1    Grossman, D.I.2    Irion, D.N.3    Schaffer, A.L.4    Eggleston, M.L.5
  • 72
    • 77952808366 scopus 로고    scopus 로고
    • Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs
    • 20441595 10.1186/1471-2156-11-35 1:CAS:528:DC%2BC3cXmtFGlsbc%3D
    • AM Oberbauer JM Belanger DI Grossman KR Regan TR Famula 2010 Genome-wide linkage scan for loci associated with epilepsy in Belgian shepherd dogs BMC Genet 11 35 20441595 10.1186/1471-2156-11-35 1:CAS:528:DC%2BC3cXmtFGlsbc%3D
    • (2010) BMC Genet , vol.11 , pp. 35
    • Oberbauer, A.M.1    Belanger, J.M.2    Grossman, D.I.3    Regan, K.R.4    Famula, T.R.5
  • 73
    • 79953735868 scopus 로고    scopus 로고
    • A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs
    • 21437276 1:CAS:528:DC%2BC3MXktVWhu7Y%3D 10.1371/journal.pgen.1001332
    • M Olsson JR Meadows K Truve G Rosengren Pielberg F Puppo, et al. 2011 A novel unstable duplication upstream of HAS2 predisposes to a breed-defining skin phenotype and a periodic fever syndrome in Chinese Shar-Pei dogs PLoS Genet 7 e1001332 21437276 1:CAS:528:DC%2BC3MXktVWhu7Y%3D 10.1371/journal.pgen.1001332
    • (2011) PLoS Genet , vol.7 , pp. 1001332
    • Olsson, M.1    Meadows, J.R.2    Truve, K.3    Rosengren Pielberg, G.4    Puppo, F.5
  • 74
    • 0033794759 scopus 로고    scopus 로고
    • Unleashing the canine genome
    • 10984444 1:CAS:528:DC%2BD3cXms1yjt7c%3D 10.1101/gr.155900
    • EA Ostrander L Kruglyak 2000 Unleashing the canine genome Genome Res 10 1271 1274 10984444 1:CAS:528:DC%2BD3cXms1yjt7c%3D 10.1101/gr.155900
    • (2000) Genome Res , vol.10 , pp. 1271-1274
    • Ostrander, E.A.1    Kruglyak, L.2
  • 75
    • 0038482140 scopus 로고    scopus 로고
    • Clinical characteristics and inheritance of idiopathic epilepsy in Vizslas
    • 12774973 10.1111/j.1939-1676.2003.tb02455.x
    • EE Patterson JR Mickelson Y Da MC Roberts AS McVey, et al. 2003 Clinical characteristics and inheritance of idiopathic epilepsy in Vizslas J Vet Intern Med 17 319 325 12774973 10.1111/j.1939-1676.2003.tb02455.x
    • (2003) J Vet Intern Med , vol.17 , pp. 319-325
    • Patterson, E.E.1    Mickelson, J.R.2    Da, Y.3    Roberts, M.C.4    McVey, A.S.5
  • 76
    • 11144310727 scopus 로고    scopus 로고
    • Clinical description and mode of inheritance of idiopathic epilepsy in English springer spaniels
    • 15646572 10.2460/javma.2005.226.54
    • EE Patterson PJ Armstrong DP O'Brien MC Roberts GS Johnson, et al. 2005 Clinical description and mode of inheritance of idiopathic epilepsy in English springer spaniels J Am Vet Med Assoc 226 54 58 15646572 10.2460/javma.2005.226. 54
    • (2005) J Am Vet Med Assoc , vol.226 , pp. 54-58
    • Patterson, E.E.1    Armstrong, P.J.2    O'Brien, D.P.3    Roberts, M.C.4    Johnson, G.S.5
  • 77
    • 52949111313 scopus 로고    scopus 로고
    • A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse
    • 18806795 1:CAS:528:DC%2BD1cXhtFKht7zL 10.1038/ng.224
    • EE Patterson KM Minor AV Tchernatynskaia SM Taylor GD Shelton, et al. 2008 A canine DNM1 mutation is highly associated with the syndrome of exercise-induced collapse Nat Genet 40 1235 1239 18806795 1:CAS:528: DC%2BD1cXhtFKht7zL 10.1038/ng.224
    • (2008) Nat Genet , vol.40 , pp. 1235-1239
    • Patterson, E.E.1    Minor, K.M.2    Tchernatynskaia, A.V.3    Taylor, S.M.4    Shelton, G.D.5
  • 78
    • 1642505430 scopus 로고    scopus 로고
    • Canine electroencephalographic recording technique: Findings in normal and epileptic dogs
    • 14744591 10.1016/S1388-2457(03)00347-X
    • FC Pellegrino RE Sica 2004 Canine electroencephalographic recording technique: findings in normal and epileptic dogs Clin Neurophysiol 115 477 487 14744591 10.1016/S1388-2457(03)00347-X
    • (2004) Clin Neurophysiol , vol.115 , pp. 477-487
    • Pellegrino, F.C.1    Sica, R.E.2
  • 79
    • 0029314484 scopus 로고
    • Seizure classification in dogs from a nonreferral-based population
    • 7782244 1:STN:280:DyaK2MzgtFCltA%3D%3D
    • M Podell WR Fenner JD Powers 1995 Seizure classification in dogs from a nonreferral-based population J Am Vet Med Assoc 206 1721 1728 7782244 1:STN:280:DyaK2MzgtFCltA%3D%3D
    • (1995) J Am Vet Med Assoc , vol.206 , pp. 1721-1728
    • Podell, M.1    Fenner, W.R.2    Powers, J.D.3
  • 80
    • 79957603217 scopus 로고    scopus 로고
    • Epilepsy genetics-past, present, and future
    • 21277190 1:CAS:528:DC%2BC3MXmvVanurg%3D 10.1016/j.gde.2011.01.005
    • A Poduri D Lowenstein 2011 Epilepsy genetics-past, present, and future Curr Opin Genet Dev 21 325 332 21277190 1:CAS:528:DC%2BC3MXmvVanurg%3D 10.1016/j.gde.2011.01.005
    • (2011) Curr Opin Genet Dev , vol.21 , pp. 325-332
    • Poduri, A.1    Lowenstein, D.2
  • 81
    • 77956210691 scopus 로고    scopus 로고
    • Absence seizures with myoclonic features in a juvenile Chihuahua dog
    • 20483714
    • R Poma A Ochi MA Cortez 2010 Absence seizures with myoclonic features in a juvenile Chihuahua dog Epileptic Disord 12 138 141 20483714
    • (2010) Epileptic Disord , vol.12 , pp. 138-141
    • Poma, R.1    Ochi, A.2    Cortez, M.A.3
  • 82
    • 0032831071 scopus 로고    scopus 로고
    • The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8
    • 10508524 1:CAS:528:DyaK1MXmtlOhuro%3D 10.1038/13868
    • S Ranta Y Zhang B Ross L Lonka E Takkunen, et al. 1999 The neuronal ceroid lipofuscinoses in human EPMR and mnd mutant mice are associated with mutations in CLN8 Nat Genet 23 233 236 10508524 1:CAS:528:DyaK1MXmtlOhuro%3D 10.1038/13868
    • (1999) Nat Genet , vol.23 , pp. 233-236
    • Ranta, S.1    Zhang, Y.2    Ross, B.3    Lonka, L.4    Takkunen, E.5
  • 83
    • 11144353883 scopus 로고    scopus 로고
    • Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy
    • 15024724 1:CAS:528:DC%2BD2cXjslGrsrc%3D 10.1002/humu.20018
    • S Ranta M Topcu S Tegelberg H Tan A Ustubutun, et al. 2004 Variant late infantile neuronal ceroid lipofuscinosis in a subset of Turkish patients is allelic to Northern epilepsy Hum Mutat 23 300 305 15024724 1:CAS:528: DC%2BD2cXjslGrsrc%3D 10.1002/humu.20018
    • (2004) Hum Mutat , vol.23 , pp. 300-305
    • Ranta, S.1    Topcu, M.2    Tegelberg, S.3    Tan, H.4    Ustubutun, A.5
  • 84
    • 33751329250 scopus 로고    scopus 로고
    • Global variation in copy number in the human genome
    • 17122850 1:CAS:528:DC%2BD28Xht1aku7zI 10.1038/nature05329
    • R Redon S Ishikawa KR Fitch L Feuk GH Perry, et al. 2006 Global variation in copy number in the human genome Nature 444 444 454 17122850 1:CAS:528:DC%2BD28Xht1aku7zI 10.1038/nature05329
    • (2006) Nature , vol.444 , pp. 444-454
    • Redon, R.1    Ishikawa, S.2    Fitch, K.R.3    Feuk, L.4    Perry, G.H.5
  • 85
    • 0025772359 scopus 로고
    • Genes for epilepsy mapped in the mouse
    • 1871601 1:CAS:528:DyaK3MXmt1Gitro%3D 10.1126/science.1871601
    • ML Rise WN Frankel JM Coffin TN Seyfried 1991 Genes for epilepsy mapped in the mouse Science 253 669 673 1871601 1:CAS:528:DyaK3MXmt1Gitro%3D 10.1126/science.1871601
    • (1991) Science , vol.253 , pp. 669-673
    • Rise, M.L.1    Frankel, W.N.2    Coffin, J.M.3    Seyfried, T.N.4
  • 86
    • 35349010252 scopus 로고    scopus 로고
    • Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs
    • 17906623 1:CAS:528:DC%2BD2sXht1aqurbO 10.1038/ng.2007.4
    • NH Salmon Hillbertz M Isaksson EK Karlsson E Hellmen GR Pielberg, et al. 2007 Duplication of FGF3, FGF4, FGF19 and ORAOV1 causes hair ridge and predisposition to dermoid sinus in Ridgeback dogs Nat Genet 39 1318 1320 17906623 1:CAS:528:DC%2BD2sXht1aqurbO 10.1038/ng.2007.4
    • (2007) Nat Genet , vol.39 , pp. 1318-1320
    • Salmon Hillbertz, N.H.1    Isaksson, M.2    Karlsson, E.K.3    Hellmen, E.4    Pielberg, G.R.5
  • 87
    • 0037398465 scopus 로고    scopus 로고
    • The epidemiology of epilepsy revisited
    • 12644744 10.1097/00019052-200304000-00008
    • JW Sander 2003 The epidemiology of epilepsy revisited Curr Opin Neurol 16 165 170 12644744 10.1097/00019052-200304000-00008
    • (2003) Curr Opin Neurol , vol.16 , pp. 165-170
    • Sander, J.W.1
  • 88
    • 77954660164 scopus 로고    scopus 로고
    • A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund
    • 20494602 1:CAS:528:DC%2BC3cXovFymtrY%3D 10.1016/j.ymgme.2010.04.009
    • DN Sanders FH Farias GS Johnson V Chiang JR Cook, et al. 2010 A mutation in canine PPT1 causes early onset neuronal ceroid lipofuscinosis in a Dachshund Mol Genet Metab 100 349 356 20494602 1:CAS:528:DC%2BC3cXovFymtrY%3D 10.1016/j.ymgme.2010.04.009
    • (2010) Mol Genet Metab , vol.100 , pp. 349-356
    • Sanders, D.N.1    Farias, F.H.2    Johnson, G.S.3    Chiang, V.4    Cook, J.R.5
  • 89
    • 33344456574 scopus 로고    scopus 로고
    • The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1
    • 16504945 1:CAS:528:DC%2BD28Xis1Gitrw%3D 10.1016/j.neuron.2006.01.033
    • U Schulte JO Thumfart N Klocker CA Sailer W Bildl, et al. 2006 The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1 Neuron 49 697 706 16504945 1:CAS:528: DC%2BD28Xis1Gitrw%3D 10.1016/j.neuron.2006.01.033
    • (2006) Neuron , vol.49 , pp. 697-706
    • Schulte, U.1    Thumfart, J.O.2    Klocker, N.3    Sailer, C.A.4    Bildl, W.5
  • 90
    • 84856057629 scopus 로고    scopus 로고
    • LGI2 truncation causes a remitting focal epilepsy in dogs
    • 21829378 1:CAS:528:DC%2BC3MXhtVOrt7vE 10.1371/journal.pgen.1002194
    • EH Seppala TS Jokinen M Fukata Y Fukata MT Webster, et al. 2011 LGI2 truncation causes a remitting focal epilepsy in dogs PLoS Genet 7 e1002194 21829378 1:CAS:528:DC%2BC3MXhtVOrt7vE 10.1371/journal.pgen.1002194
    • (2011) PLoS Genet , vol.7 , pp. 1002194
    • Seppala, E.H.1    Jokinen, T.S.2    Fukata, M.3    Fukata, Y.4    Webster, M.T.5
  • 91
    • 0029082843 scopus 로고
    • The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q
    • 8541857 1:CAS:528:DyaK2MXnvVentrs%3D 10.1093/hmg/4.9.1657
    • JM Serratosa AV Delgado-Escueta I Posada S Shih I Drury, et al. 1995 The gene for progressive myoclonus epilepsy of the Lafora type maps to chromosome 6q Hum Mol Genet 4 1657 1663 8541857 1:CAS:528:DyaK2MXnvVentrs%3D 10.1093/hmg/4.9.1657
    • (1995) Hum Mol Genet , vol.4 , pp. 1657-1663
    • Serratosa, J.M.1    Delgado-Escueta, A.V.2    Posada, I.3    Shih, S.4    Drury, I.5
  • 92
    • 33745079623 scopus 로고    scopus 로고
    • Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis
    • 16670177 10.1093/brain/awl107
    • E Siintola S Partanen P Stromme A Haapanen M Haltia, et al. 2006 Cathepsin D deficiency underlies congenital human neuronal ceroid-lipofuscinosis Brain 129 1438 1445 16670177 10.1093/brain/awl107
    • (2006) Brain , vol.129 , pp. 1438-1445
    • Siintola, E.1    Partanen, S.2    Stromme, P.3    Haapanen, A.4    Haltia, M.5
  • 93
    • 0032055649 scopus 로고    scopus 로고
    • Deletion of the K(V)1.1 potassium channel causes epilepsy in mice
    • 9581771 1:CAS:528:DyaK1cXivVCju74%3D 10.1016/S0896-6273(00)81018-1
    • SL Smart V Lopantsev CL Zhang CA Robbins H Wang, et al. 1998 Deletion of the K(V)1.1 potassium channel causes epilepsy in mice Neuron 20 809 819 9581771 1:CAS:528:DyaK1cXivVCju74%3D 10.1016/S0896-6273(00)81018-1
    • (1998) Neuron , vol.20 , pp. 809-819
    • Smart, S.L.1    Lopantsev, V.2    Zhang, C.L.3    Robbins, C.A.4    Wang, H.5
  • 94
    • 0028724590 scopus 로고
    • Genetic basis of idiopathic epilepsy in the golden retriever
    • 7716756 1:STN:280:DyaK2M3jt1Omtw%3D%3D
    • P Srenk A Jaggy C Gaillard A Busato P Horin 1994 Genetic basis of idiopathic epilepsy in the golden retriever Tierarztl Prax 22 574 578 7716756 1:STN:280:DyaK2M3jt1Omtw%3D%3D
    • (1994) Tierarztl Prax , vol.22 , pp. 574-578
    • Srenk, P.1    Jaggy, A.2    Gaillard, C.3    Busato, A.4    Horin, P.5
  • 95
    • 33646871344 scopus 로고    scopus 로고
    • Cathepsin D deficiency is associated with a human neurodegenerative disorder
    • 16685649 1:CAS:528:DC%2BD28XltVyks78%3D 10.1086/504159
    • R Steinfeld K Reinhardt K Schreiber M Hillebrand R Kraetzner, et al. 2006 Cathepsin D deficiency is associated with a human neurodegenerative disorder Am J Hum Genet 78 988 998 16685649 1:CAS:528:DC%2BD28XltVyks78%3D 10.1086/504159
    • (2006) Am J Hum Genet , vol.78 , pp. 988-998
    • Steinfeld, R.1    Reinhardt, K.2    Schreiber, K.3    Hillebrand, M.4    Kraetzner, R.5
  • 96
    • 0032769260 scopus 로고    scopus 로고
    • Idiopathic epilepsies with a monogenic mode of inheritance
    • 10446744 1:CAS:528:DyaK1MXmt1Wlsbs%3D 10.1111/j.1528-1157.1999.tb00892.x
    • OK Steinlein 1999 Idiopathic epilepsies with a monogenic mode of inheritance Epilepsia 40 Suppl 3 9 11 10446744 1:CAS:528:DyaK1MXmt1Wlsbs%3D 10.1111/j.1528-1157.1999.tb00892.x
    • (1999) Epilepsia , vol.40 , Issue.SUPPL. 3 , pp. 9-11
    • Steinlein, O.K.1
  • 97
    • 0033978781 scopus 로고    scopus 로고
    • Idiopathic epilepsy in dogs
    • 10680215 1:STN:280:DC%2BD3c7ksVCltQ%3D%3D vii
    • WB Thomas 2000 Idiopathic epilepsy in dogs Vet Clin North Am Small Anim Pract 30 183 206 10680215 1:STN:280:DC%2BD3c7ksVCltQ%3D%3D vii
    • (2000) Vet Clin North Am Small Anim Pract , vol.30 , pp. 183-206
    • Thomas, W.B.1
  • 98
    • 71749119354 scopus 로고    scopus 로고
    • Idiopathic epilepsy in dogs and cats
    • 19942062 10.1016/j.cvsm.2009.09.004
    • WB Thomas 2010 Idiopathic epilepsy in dogs and cats Vet Clin North Am Small Anim Pract 40 161 179 19942062 10.1016/j.cvsm.2009.09.004
    • (2010) Vet Clin North Am Small Anim Pract , vol.40 , pp. 161-179
    • Thomas, W.B.1
  • 99
    • 84884465389 scopus 로고    scopus 로고
    • Convulsive disorders
    • J.G. Fox S.W. Barthold M.T. Davisson C.E. Newcomer F.W. Quimby A.L. Smith (eds). Academic Press Burlington
    • Todorova MT, Seyfried TN (2006) Convulsive disorders. In: Fox JG, Barthold SW, Davisson MT, Newcomer CE, Quimby FW, Smith AL (eds) The mouse in biomedical research, chap 17. Academic Press, Burlington, pp 565-594
    • (2006) The Mouse in Biomedical Research, Chap 17 , pp. 565-594
    • Todorova, M.T.1    Seyfried, T.N.2
  • 101
    • 33645651294 scopus 로고    scopus 로고
    • Magnetic resonance imaging findings in Finnish Spitz dogs with focal epilepsy
    • 16594587 1:STN:280:DC%2BD287ovFensg%3D%3D 10.1111/j.1939-1676.2006. tb02861.x
    • R Viitmaa S Cizinauskas LA Bergamasco E Kuusela P Pascoe, et al. 2006 Magnetic resonance imaging findings in Finnish Spitz dogs with focal epilepsy J Vet Intern Med 20 305 310 16594587 1:STN:280:DC%2BD287ovFensg%3D%3D 10.1111/j.1939-1676.2006.tb02861.x
    • (2006) J Vet Intern Med , vol.20 , pp. 305-310
    • Viitmaa, R.1    Cizinauskas, S.2    Bergamasco, L.A.3    Kuusela, E.4    Pascoe, P.5
  • 102
    • 0016669711 scopus 로고
    • Keeshonds: A genetic study of epilepsy and EEG readings
    • 1117701 1:STN:280:DyaE2M7hslKksg%3D%3D 10.1111/j.1748-5827.1975.tb05709.x
    • ME Wallace 1975 Keeshonds: a genetic study of epilepsy and EEG readings J Small Anim Pract 16 1 10 1117701 1:STN:280:DyaE2M7hslKksg%3D%3D 10.1111/j.1748-5827.1975.tb05709.x
    • (1975) J Small Anim Pract , vol.16 , pp. 1-10
    • Wallace, M.E.1
  • 103
    • 17344367657 scopus 로고    scopus 로고
    • Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B
    • 9697698 1:CAS:528:DyaK1cXls1Cktb0%3D 10.1038/448
    • RH Wallace DW Wang R Singh IE Scheffer AL George Jr, et al. 1998 Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B Nat Genet 19 366 370 9697698 1:CAS:528: DyaK1cXls1Cktb0%3D 10.1038/448
    • (1998) Nat Genet , vol.19 , pp. 366-370
    • Wallace, R.H.1    Wang, D.W.2    Singh, R.3    Scheffer, I.E.4    George Jr., A.L.5
  • 104
    • 0035033520 scopus 로고    scopus 로고
    • Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures
    • 11326275 1:CAS:528:DC%2BD3MXjt1Wqu7o%3D
    • RH Wallace C Marini S Petrou LA Harkin DN Bowser, et al. 2001 Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures Nat Genet 28 49 52 11326275 1:CAS:528:DC%2BD3MXjt1Wqu7o%3D
    • (2001) Nat Genet , vol.28 , pp. 49-52
    • Wallace, R.H.1    Marini, C.2    Petrou, S.3    Harkin, L.A.4    Bowser, D.N.5
  • 105
    • 77649188325 scopus 로고    scopus 로고
    • Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex
    • 20101241 1:CAS:528:DC%2BC3cXhtVWrtbc%3D 10.1038/ng.525
    • M Wilbe P Jokinen K Truve EH Seppala EK Karlsson, et al. 2010 Genome-wide association mapping identifies multiple loci for a canine SLE-related disease complex Nat Genet 42 250 254 20101241 1:CAS:528:DC%2BC3cXhtVWrtbc%3D 10.1038/ng.525
    • (2010) Nat Genet , vol.42 , pp. 250-254
    • Wilbe, M.1    Jokinen, P.2    Truve, K.3    Seppala, E.H.4    Karlsson, E.K.5
  • 106
    • 33846006596 scopus 로고    scopus 로고
    • A comprehensive analysis of common copy-number variations in the human genome
    • 17160897 1:CAS:528:DC%2BD2sXms1CmsA%3D%3D 10.1086/510560
    • KK Wong RJ deLeeuw NS Dosanjh LR Kimm Z Cheng, et al. 2007 A comprehensive analysis of common copy-number variations in the human genome Am J Hum Genet 80 91 104 17160897 1:CAS:528:DC%2BD2sXms1CmsA%3D%3D 10.1086/510560
    • (2007) Am J Hum Genet , vol.80 , pp. 91-104
    • Wong, K.K.1    Deleeuw, R.J.2    Dosanjh, N.S.3    Kimm, L.R.4    Cheng, Z.5
  • 107
    • 70350494929 scopus 로고    scopus 로고
    • Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy
    • 19701204 1:CAS:528:DC%2BD1MXhtVersbrM 10.1038/nm.2019
    • YD Zhou S Lee Z Jin M Wright SEP Smith, et al. 2009 Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy Nat Med 15 1208 1214 19701204 1:CAS:528:DC%2BD1MXhtVersbrM 10.1038/nm.2019
    • (2009) Nat Med , vol.15 , pp. 1208-1214
    • Zhou, Y.D.1    Lee, S.2    Jin, Z.3    Wright, M.4    Smith, S.E.P.5
  • 108
    • 0032895470 scopus 로고    scopus 로고
    • A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy
    • 10355668 10.1093/brain/122.5.817
    • SM Zuberi LH Eunson A Spauschus R De Silva J Tolmie, et al. 1999 A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy Brain 122 Pt 5 817 825 10355668 10.1093/brain/122.5.817
    • (1999) Brain , vol.122 , Issue.PART 5 , pp. 817-825
    • Zuberi, S.M.1    Eunson, L.H.2    Spauschus, A.3    De Silva, R.4    Tolmie, J.5


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