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Volumn 103, Issue , 2012, Pages 451-459

Spinocerebellar ataxia type 5

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EID: 79961153510     PISSN: 00729752     EISSN: None     Source Type: Book Series    
DOI: 10.1016/B978-0-444-51892-7.00028-0     Document Type: Chapter
Times cited : (29)

References (48)
  • 1
    • 0036340697 scopus 로고    scopus 로고
    • A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter
    • Brkanac Z., Bylenok L., Fernandez M., et al. A new dominant spinocerebellar ataxia linked to chromosome 19q13.4-qter. Arch Neurol 2002, 59:1291-1295.
    • (2002) Arch Neurol , vol.59 , pp. 1291-1295
    • Brkanac, Z.1    Bylenok, L.2    Fernandez, M.3
  • 2
    • 0842347338 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred
    • Burk K., Zuhlke C., Konig I.R., et al. Spinocerebellar ataxia type 5: clinical and molecular genetic features of a German kindred. Neurology 2004, 62:327-329.
    • (2004) Neurology , vol.62 , pp. 327-329
    • Burk, K.1    Zuhlke, C.2    Konig, I.R.3
  • 3
    • 30344475206 scopus 로고    scopus 로고
    • SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2
    • Cagnoli C., Mariotti C., Taroni F., et al. SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2. Brain 2006, 129:235-242.
    • (2006) Brain , vol.129 , pp. 235-242
    • Cagnoli, C.1    Mariotti, C.2    Taroni, F.3
  • 4
    • 0037385006 scopus 로고    scopus 로고
    • Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia
    • Chen D.H., Brkanac Z., Verlinde C.L., et al. Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia. Am J Hum Genet 2003, 72:839-849.
    • (2003) Am J Hum Genet , vol.72 , pp. 839-849
    • Chen, D.H.1    Brkanac, Z.2    Verlinde, C.L.3
  • 5
    • 0037677603 scopus 로고    scopus 로고
    • A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23
    • Chung M.Y., Lu Y.C., Cheng N.C., et al. A novel autosomal dominant spinocerebellar ataxia (SCA22) linked to chromosome 1p21-q23. Brain 2003, 126:1293-1299.
    • (2003) Brain , vol.126 , pp. 1293-1299
    • Chung, M.Y.1    Lu, Y.C.2    Cheng, N.C.3
  • 6
    • 33745088678 scopus 로고    scopus 로고
    • Molecular pathogenesis of spinocerebellar ataxias
    • Duenas A.M., Goold R., Giunti P. Molecular pathogenesis of spinocerebellar ataxias. Brain 2006, 129:1357-1370.
    • (2006) Brain , vol.129 , pp. 1357-1370
    • Duenas, A.M.1    Goold, R.2    Giunti, P.3
  • 7
    • 0001172320 scopus 로고
    • Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred
    • Gardner K., Alderson K., Galster B., et al. Autosomal dominant spinocerebellar ataxia: clinical description of a distinct hereditary ataxia and genetic localization to chromosome 16 (SCA4) in a Utah kindred. Neurology 1994, 44:A361.
    • (1994) Neurology , vol.44
    • Gardner, K.1    Alderson, K.2    Galster, B.3
  • 8
    • 3142636768 scopus 로고    scopus 로고
    • Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules
    • Gauthier L.R., Charrin B.C., Borrell-Pages M., et al. Huntingtin controls neurotrophic support and survival of neurons by enhancing BDNF vesicular transport along microtubules. Cell 2004, 118:127-138.
    • (2004) Cell , vol.118 , pp. 127-138
    • Gauthier, L.R.1    Charrin, B.C.2    Borrell-Pages, M.3
  • 9
    • 0037734370 scopus 로고    scopus 로고
    • Mutations in dynein link motor neuron degeneration to defects in retrograde transport
    • Hafezparast M., Klocke R., Ruhrberg C., et al. Mutations in dynein link motor neuron degeneration to defects in retrograde transport. Science 2003, 300:808-812.
    • (2003) Science , vol.300 , pp. 808-812
    • Hafezparast, M.1    Klocke, R.2    Ruhrberg, C.3
  • 10
    • 0032858354 scopus 로고    scopus 로고
    • Interaction of the C-terminal domain of delta glutamate receptor with spectrin in the dendritic spines of cultured Purkinje cells
    • Hirai H., Matsuda S. Interaction of the C-terminal domain of delta glutamate receptor with spectrin in the dendritic spines of cultured Purkinje cells. Neurosci Res 1999, 34:281-287.
    • (1999) Neurosci Res , vol.34 , pp. 281-287
    • Hirai, H.1    Matsuda, S.2
  • 11
    • 0035965256 scopus 로고    scopus 로고
    • Beta III spectrin binds to the Arp1 subunit of dynactin
    • Holleran E.A., Ligon L.A., Tokito M., et al. Beta III spectrin binds to the Arp1 subunit of dynactin. J Biol Chem 2001, 276:36598-36605.
    • (2001) J Biol Chem , vol.276 , pp. 36598-36605
    • Holleran, E.A.1    Ligon, L.A.2    Tokito, M.3
  • 12
    • 0032727249 scopus 로고    scopus 로고
    • Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12
    • Holmes S.E., O'Hearn E.E., McInnis M.G., et al. Expansion of a novel CAG trinucleotide repeat in the 5' region of PPP2R2B is associated with SCA12. Nat Genet 1999, 23:391-392.
    • (1999) Nat Genet , vol.23 , pp. 391-392
    • Holmes, S.E.1    O'Hearn, E.E.2    McInnis, M.G.3
  • 13
    • 31744441984 scopus 로고    scopus 로고
    • Spectrin mutations cause spinocerebellar ataxia type 5
    • Ikeda Y., Dick K.A., Weatherspoon M.R., et al. Spectrin mutations cause spinocerebellar ataxia type 5. Nat Genet 2006, 38:184-190.
    • (2006) Nat Genet , vol.38 , pp. 184-190
    • Ikeda, Y.1    Dick, K.A.2    Weatherspoon, M.R.3
  • 14
    • 0035282328 scopus 로고    scopus 로고
    • Modulation of the neuronal glutamate transporter EAAT4 by two interacting proteins
    • Jackson M., Song W., Liu M.Y., et al. Modulation of the neuronal glutamate transporter EAAT4 by two interacting proteins. Nature 2001, 410:89-93.
    • (2001) Nature , vol.410 , pp. 89-93
    • Jackson, M.1    Song, W.2    Liu, M.Y.3
  • 15
    • 0038048459 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant
    • Knight M.A., Kennerson M.L., Anney R.J., et al. Spinocerebellar ataxia type 15 (sca15) maps to 3p24.2-3pter: exclusion of the ITPR1 gene, the human orthologue of an ataxic mouse mutant. Neurobiol Dis 2003, 13:147-157.
    • (2003) Neurobiol Dis , vol.13 , pp. 147-157
    • Knight, M.A.1    Kennerson, M.L.2    Anney, R.J.3
  • 16
    • 2442527917 scopus 로고    scopus 로고
    • Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20
    • Knight M.A., Gardner R.J., Bahlo M., et al. Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20. Brain 2004, 127:1172-1181.
    • (2004) Brain , vol.127 , pp. 1172-1181
    • Knight, M.A.1    Gardner, R.J.2    Bahlo, M.3
  • 17
    • 0345199753 scopus 로고
    • High-resolution genetic and physical mapping of spinocerebellar ataxia type 5 (SCA5) on 11q13
    • Koob M.J., Lundgren N., Nowak T., et al. High-resolution genetic and physical mapping of spinocerebellar ataxia type 5 (SCA5) on 11q13. Am J Hum Genet 1995, 57:A196.
    • (1995) Am J Hum Genet , vol.57
    • Koob, M.J.1    Lundgren, N.2    Nowak, T.3
  • 18
    • 0025762012 scopus 로고
    • Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment
    • Krawczak M., Cooper D.N. Gene deletions causing human genetic disease: mechanisms of mutagenesis and the role of the local DNA sequence environment. Hum Genet 1991, 86:425-441.
    • (1991) Hum Genet , vol.86 , pp. 425-441
    • Krawczak, M.1    Cooper, D.N.2
  • 19
    • 0032524625 scopus 로고    scopus 로고
    • Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher
    • Lalouette A., Guenet J.L., Vriz S. Hotfoot mouse mutations affect the delta 2 glutamate receptor gene and are allelic to lurcher. Genomics 1998, 50:9-13.
    • (1998) Genomics , vol.50 , pp. 9-13
    • Lalouette, A.1    Guenet, J.L.2    Vriz, S.3
  • 20
    • 0033995175 scopus 로고    scopus 로고
    • Polyglutamine expansion down- regulates specific neuronal genes before pathologic changes in SCA1
    • Lin X., Antalffy B., Kang D., et al. Polyglutamine expansion down- regulates specific neuronal genes before pathologic changes in SCA1. Nat Neurosci 2000, 3:157-163.
    • (2000) Nat Neurosci , vol.3 , pp. 157-163
    • Lin, X.1    Antalffy, B.2    Kang, D.3
  • 21
    • 31744440601 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 5 (SCA5)
    • Cambridge University Press, Cambridge, M. Pandolfo (Ed.)
    • Liquori C., Schut L.J., Clark H.B., et al. Spinocerebellar ataxia type 5 (SCA5). Cerebellar Ataxias 2002, 445-450. Cambridge University Press, Cambridge. M. Pandolfo (Ed.).
    • (2002) Cerebellar Ataxias , pp. 445-450
    • Liquori, C.1    Schut, L.J.2    Clark, H.B.3
  • 22
    • 0033771685 scopus 로고    scopus 로고
    • Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10
    • Matsuura T., Yamagata T., Burgess D.L., et al. Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10. Nat Genet 2000, 26:191-194.
    • (2000) Nat Genet , vol.26 , pp. 191-194
    • Matsuura, T.1    Yamagata, T.2    Burgess, D.L.3
  • 23
    • 0035838438 scopus 로고    scopus 로고
    • A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1
    • Miyoshi Y., Yamada T., Tanimura M., et al. A novel autosomal dominant spinocerebellar ataxia (SCA16) linked to chromosome 8q22.1-24.1. Neurology 2001, 57:96-100.
    • (2001) Neurology , vol.57 , pp. 96-100
    • Miyoshi, Y.1    Yamada, T.2    Tanimura, M.3
  • 24
    • 33745545413 scopus 로고    scopus 로고
    • Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8
    • Moseley M.L., Zu T., Ikeda Y. Bidirectional expression of CUG and CAG expansion transcripts and intranuclear polyglutamine inclusions in spinocerebellar ataxia type 8. Nat Genet 2006, 38:758-769.
    • (2006) Nat Genet , vol.38 , pp. 758-769
    • Moseley, M.L.1    Zu, T.2    Ikeda, Y.3
  • 25
    • 0032526226 scopus 로고    scopus 로고
    • Characterization of a new beta-spectrin gene which is predominantly expressed in brain
    • Ohara O., Ohara R., Yamakawa H., et al. Characterization of a new beta-spectrin gene which is predominantly expressed in brain. Brain Res Mol Brain Res 1998, 57:181-192.
    • (1998) Brain Res Mol Brain Res , vol.57 , pp. 181-192
    • Ohara, O.1    Ohara, R.2    Yamakawa, H.3
  • 26
    • 0022476162 scopus 로고
    • Mutations with dominant effects on the behavior and morphology of the nematode Caenorhabditis elegans
    • Park E.C., Horvitz H.R. Mutations with dominant effects on the behavior and morphology of the nematode Caenorhabditis elegans. Genetics 1986, 113:821-852.
    • (1986) Genetics , vol.113 , pp. 821-852
    • Park, E.C.1    Horvitz, H.R.2
  • 27
    • 0034863510 scopus 로고    scopus 로고
    • Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice
    • Parkinson N.J., Olsson C.L., Hallows J.L., et al. Mutant beta-spectrin 4 causes auditory and motor neuropathies in quivering mice. Nat Genet 2001, 29:61-65.
    • (2001) Nat Genet , vol.29 , pp. 61-65
    • Parkinson, N.J.1    Olsson, C.L.2    Hallows, J.L.3
  • 28
    • 0034691599 scopus 로고    scopus 로고
    • A protein accumulator
    • Pinder J.C., Baines A.J. A protein accumulator. Nature 2000, 406:253-254.
    • (2000) Nature , vol.406 , pp. 253-254
    • Pinder, J.C.1    Baines, A.J.2
  • 29
    • 0037382240 scopus 로고    scopus 로고
    • Mutant dynactin in motor neuron disease
    • Puls I., Jonnakuty C., LaMonte B.H., et al. Mutant dynactin in motor neuron disease. Nat Genet 2003, 33:455-456.
    • (2003) Nat Genet , vol.33 , pp. 455-456
    • Puls, I.1    Jonnakuty, C.2    LaMonte, B.H.3
  • 30
    • 0036866156 scopus 로고    scopus 로고
    • Coexistence and function of different neurotransmitter transporters in the plasma membrane of CNS neurons
    • Raiteri L., Raiteri M., Bonanno G. Coexistence and function of different neurotransmitter transporters in the plasma membrane of CNS neurons. Prog Neurobiol 2002, 68:287-309.
    • (2002) Prog Neurobiol , vol.68 , pp. 287-309
    • Raiteri, L.1    Raiteri, M.2    Bonanno, G.3
  • 31
    • 0028020605 scopus 로고
    • A dominant spinocerebellar ataxia gene (SCA5) in a family descendent from the paternal grandparents of President Lincoln maps to chromosome 11
    • Ranum L.P.W., Schut L.J., Lundgren J.K., et al. A dominant spinocerebellar ataxia gene (SCA5) in a family descendent from the paternal grandparents of President Lincoln maps to chromosome 11. Nat Genet 1994, 8:280-284.
    • (1994) Nat Genet , vol.8 , pp. 280-284
    • Ranum, L.P.W.1    Schut, L.J.2    Lundgren, J.K.3
  • 32
    • 79961159712 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 5
    • Marcel Dekker, New York, T. Klockgether (Ed.)
    • Schut L.J., Day J.W., Clark H.B., et al. Spinocerebellar ataxia type 5. Handbook of Ataxia Disorders 2000, 435-445. Marcel Dekker, New York. T. Klockgether (Ed.).
    • (2000) Handbook of Ataxia Disorders , pp. 435-445
    • Schut, L.J.1    Day, J.W.2    Clark, H.B.3
  • 33
    • 19544374135 scopus 로고    scopus 로고
    • Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice
    • Serra H.G., Byam C.E., Lande J.D., et al. Gene profiling links SCA1 pathophysiology to glutamate signaling in Purkinje cells of transgenic mice. Hum Mol Genet 2004, 13:2535-2543.
    • (2004) Hum Mol Genet , vol.13 , pp. 2535-2543
    • Serra, H.G.1    Byam, C.E.2    Lande, J.D.3
  • 34
    • 0034647753 scopus 로고    scopus 로고
    • Identification and characterization of beta V spectrin, a mammalian ortholog of Drosophila beta H spectrin
    • Stabach P.R., Morrow J.S. Identification and characterization of beta V spectrin, a mammalian ortholog of Drosophila beta H spectrin. J Biol Chem 2000, 275:21385-21395.
    • (2000) J Biol Chem , vol.275 , pp. 21385-21395
    • Stabach, P.R.1    Morrow, J.S.2
  • 35
    • 0032564278 scopus 로고    scopus 로고
    • A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles
    • Stankewich M.C., Tse W.T., Peters L.L., et al. A widely expressed betaIII spectrin associated with Golgi and cytoplasmic vesicles. Proc Natl Acad Sci U S A 1998, 95:14158-14163.
    • (1998) Proc Natl Acad Sci U S A , vol.95 , pp. 14158-14163
    • Stankewich, M.C.1    Tse, W.T.2    Peters, L.L.3
  • 36
    • 0032834350 scopus 로고    scopus 로고
    • Clinical and MRI findings in spinocerebellar ataxia type 5
    • Stevanin G., Herman A., Brice A., et al. Clinical and MRI findings in spinocerebellar ataxia type 5. Neurology 1999, 53:1355-1357.
    • (1999) Neurology , vol.53 , pp. 1355-1357
    • Stevanin, G.1    Herman, A.2    Brice, A.3
  • 37
    • 9144256120 scopus 로고    scopus 로고
    • Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p
    • Stevanin G., Bouslam N., Thobois S., et al. Spinocerebellar ataxia with sensory neuropathy (SCA25) maps to chromosome 2p. Ann Neurol 2004, 55:97-104.
    • (2004) Ann Neurol , vol.55 , pp. 97-104
    • Stevanin, G.1    Bouslam, N.2    Thobois, S.3
  • 38
    • 0036237387 scopus 로고    scopus 로고
    • A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus
    • Swartz B.E., Burmeister M., Somers J.T., et al. A form of inherited cerebellar ataxia with saccadic intrusions, increased saccadic speed, sensory neuropathy, and myoclonus. Ann N Y Acad Sci 2002, 956:441-444.
    • (2002) Ann N Y Acad Sci , vol.956 , pp. 441-444
    • Swartz, B.E.1    Burmeister, M.2    Somers, J.T.3
  • 39
    • 0037219826 scopus 로고    scopus 로고
    • A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]
    • van Swieten J.C., Brusse E., de Graaf B.M., et al. A mutation in the fibroblast growth factor 14 gene is associated with autosomal dominant cerebellar ataxia [corrected]. Am J Hum Genet 2003, 72:191-199.
    • (2003) Am J Hum Genet , vol.72 , pp. 191-199
    • van Swieten, J.C.1    Brusse, E.2    de Graaf, B.M.3
  • 40
    • 0036820509 scopus 로고    scopus 로고
    • Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21
    • Verbeek D.S., Schelhaas J.H., Ippel E.F., et al. Identification of a novel SCA locus (SCA19) in a Dutch autosomal dominant cerebellar ataxia family on chromosome region 1p21-q21. Hum Genet 2002, 111:388-393.
    • (2002) Hum Genet , vol.111 , pp. 388-393
    • Verbeek, D.S.1    Schelhaas, J.H.2    Ippel, E.F.3
  • 41
    • 8144221193 scopus 로고    scopus 로고
    • Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3
    • Verbeek D.S., van de War enburg B.P., Wesseling P., et al. Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3. Brain 2004, 127:2551-2557.
    • (2004) Brain , vol.127 , pp. 2551-2557
    • Verbeek, D.S.1    van de War enburg, B.P.2    Wesseling, P.3
  • 42
    • 0036830123 scopus 로고    scopus 로고
    • A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1
    • Vuillaume I., Devos D., Schraen-Maschke S., et al. A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1. Ann Neurol 2002, 52:666-670.
    • (2002) Ann Neurol , vol.52 , pp. 666-670
    • Vuillaume, I.1    Devos, D.2    Schraen-Maschke, S.3
  • 43
    • 33645421783 scopus 로고    scopus 로고
    • Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes
    • Waters M.F., Minassian N.A., Stevanin G., et al. Mutations in voltage-gated potassium channel KCNC3 cause degenerative and developmental central nervous system phenotypes. Nat Genet 2006, 38:447-451.
    • (2006) Nat Genet , vol.38 , pp. 447-451
    • Waters, M.F.1    Minassian, N.A.2    Stevanin, G.3
  • 44
    • 0036366704 scopus 로고    scopus 로고
    • Why do Purkinje cells die so easily after global brain ischemia? Aldolase C, EAAT4, and the cerebellar contribution to posthypoxic myoclonus
    • Welsh J.P., Yuen G., Placantonakis D.G., et al. Why do Purkinje cells die so easily after global brain ischemia? Aldolase C, EAAT4, and the cerebellar contribution to posthypoxic myoclonus. Adv Neurol 2002, 89:331-359.
    • (2002) Adv Neurol , vol.89 , pp. 331-359
    • Welsh, J.P.1    Yuen, G.2    Placantonakis, D.G.3
  • 45
    • 0033358555 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cm region on chromosome 15q14-21.3
    • Worth P.F., Giunti P., Gardner-Thorpe C., et al. Autosomal dominant cerebellar ataxia type III: linkage in a large British family to a 7.6-cm region on chromosome 15q14-21.3. Am J Hum Genet 1999, 65:420-426.
    • (1999) Am J Hum Genet , vol.65 , pp. 420-426
    • Worth, P.F.1    Giunti, P.2    Gardner-Thorpe, C.3
  • 46
    • 14844297397 scopus 로고    scopus 로고
    • Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6
    • Yu G.Y., Howell M.J., Roller M.J., et al. Spinocerebellar ataxia type 26 maps to chromosome 19p13.3 adjacent to SCA6. Ann Neurol 2005, 57:349-354.
    • (2005) Ann Neurol , vol.57 , pp. 349-354
    • Yu, G.Y.1    Howell, M.J.2    Roller, M.J.3
  • 47
    • 0031012399 scopus 로고    scopus 로고
    • Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha-1A-voltage-dependent calcium channel
    • Zhuchenko O., Bailey J., Bonnen P., et al. Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha-1A-voltage-dependent calcium channel. Nat Genet 1997, 15:62-69.
    • (1997) Nat Genet , vol.15 , pp. 62-69
    • Zhuchenko, O.1    Bailey, J.2    Bonnen, P.3
  • 48
    • 0030800468 scopus 로고    scopus 로고
    • Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene
    • Zuo J., De Jager P.L., Takahashi K.A., et al. Neurodegeneration in Lurcher mice caused by mutation in delta2 glutamate receptor gene. Nature 1997, 388:769-773.
    • (1997) Nature , vol.388 , pp. 769-773
    • Zuo, J.1    De Jager, P.L.2    Takahashi, K.A.3


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