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Volumn 19, Issue 4, 1999, Pages 353-362

Inherited peripheral neuropathy

Author keywords

Charcot Marie Tooth neuropathy (CMT); Dejerine Sottas disease; Peripheral neuropathy

Indexed keywords

CONNEXIN 32; GENE PRODUCT; MYELIN PROTEIN;

EID: 0033400053     PISSN: 02718235     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1040850     Document Type: Review
Times cited : (33)

References (110)
  • 1
    • 0016266593 scopus 로고
    • Genetic and clinical aspects of Charcot-Marie-Tooth's disease
    • Skre H. Genetic and clinical aspects of Charcot-Marie-Tooth's disease. Clin Genet 1974;6:98-118
    • (1974) Clin Genet , vol.6 , pp. 98-118
    • Skre, H.1
  • 2
    • 0001046663 scopus 로고
    • Hereditary motor and sensory neuropathies
    • Dyck PJ, Thomas PJ, Griffin JW, Low PA, Poduslo JF, eds. Philadelphia: WB Saunders
    • Dyck PJ, Chance PF, Leho RV, Carney JA. Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PJ, Griffin JW, Low PA, Poduslo JF, eds. Peripheral Neuropathy. Philadelphia: WB Saunders, 1993:1094-1136
    • (1993) Peripheral Neuropathy , pp. 1094-1136
    • Dyck, P.J.1    Chance, P.F.2    Leho, R.V.3    Carney, J.A.4
  • 4
    • 0025224806 scopus 로고
    • Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I)
    • Chance PF, Bird TD, O'Connell P, Lipe H, Lalouel JM, Leppert M. Genetic linkage and heterogeneity in type I Charcot-Marie-Tooth disease (hereditary motor and sensory neuropathy type I). Am J Hum Genet 1990;47:915-925
    • (1990) Am J Hum Genet , vol.47 , pp. 915-925
    • Chance, P.F.1    Bird, T.D.2    O'Connell, P.3    Lipe, H.4    Lalouel, J.M.5    Leppert, M.6
  • 5
    • 0025024576 scopus 로고
    • Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17
    • McAlpine PJ, Feasby TE, Hahn AF, Komarnicki L, James S, Guy C, et al. Localization of a locus for Charcot-Marie-Tooth neuropathy type Ia (CMT1A) to chromosome 17. Genomics 1990;7:408-415
    • (1990) Genomics , vol.7 , pp. 408-415
    • McAlpine, P.J.1    Feasby, T.E.2    Hahn, A.F.3    Komarnicki, L.4    James, S.5    Guy, C.6
  • 6
    • 0025169909 scopus 로고
    • Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17
    • Middleton-Price HR, Harding AE, Monteiro C, Berciano J, Malcolm S. Linkage of hereditary motor and sensory neuropathy type I to the pericentromeric region of chromosome 17. Am J Hum Genet 1990;46:92-94
    • (1990) Am J Hum Genet , vol.46 , pp. 92-94
    • Middleton-Price, H.R.1    Harding, A.E.2    Monteiro, C.3    Berciano, J.4    Malcolm, S.5
  • 7
    • 0025344688 scopus 로고
    • Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: Identification of new linked markers on chromosome
    • Patel PI, Franco B, Garcia C, Slaugenhaupt SA, Nakamura Y, Ledbetter DH, et al. Genetic mapping of autosomal dominant Charcot-Marie-Tooth disease in a large French-Acadian kindred: Identification of new linked markers on chromosome. Am J Hum Genet 1990;46:801-809
    • (1990) Am J Hum Genet , vol.46 , pp. 801-809
    • Patel, P.I.1    Franco, B.2    Garcia, C.3    Slaugenhaupt, S.A.4    Nakamura, Y.5    Ledbetter, D.H.6
  • 8
    • 0025976006 scopus 로고
    • Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2
    • Vance JM, Barker D, Yamaoka LH, Stajich JM, Loprest L, Hung WY, et al. Localization of Charcot-Marie-Tooth disease type 1a (CMT1A) to chromosome 17p11.2. Genomics 1991;9:623-628
    • (1991) Genomics , vol.9 , pp. 623-628
    • Vance, J.M.1    Barker, D.2    Yamaoka, L.H.3    Stajich, J.M.4    Loprest, L.5    Hung, W.Y.6
  • 10
    • 0026564694 scopus 로고
    • Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group
    • Raeymaekers P. Timmerman V, Nelis E, Van Hul W, De Jonghe P, Martin J, et al. Estimation of the size of the chromosome 17p11.2 duplication in Charcot-Marie-Tooth neuropathy type 1a (CMT1a). HMSN Collaborative Research Group. J Med Genet 1992;29:5-11
    • (1992) J Med Genet , vol.29 , pp. 5-11
    • Raeymaekers, P.1    Timmerman, V.2    Nelis, E.3    Van Hul, W.4    De Jonghe, P.5    Martin, J.6
  • 14
    • 0030030169 scopus 로고    scopus 로고
    • Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1A: First report of a de novo duplication with a maternal origin
    • Blair IP, Nash J, Gordon MJ, Nicholson GA. Prevalence and origin of de novo duplications in Charcot-Marie-Tooth disease type 1A: First report of a de novo duplication with a maternal origin. Am J Hum Genet 1996;58:472-476
    • (1996) Am J Hum Genet , vol.58 , pp. 472-476
    • Blair, I.P.1    Nash, J.2    Gordon, M.J.3    Nicholson, G.A.4
  • 15
    • 65749318026 scopus 로고
    • Two new mutants, "Trembler" and "Reeler" with neurological actions in the mouse (Mus musculus L.)
    • Falconer DS. Two new mutants, "Trembler" and "Reeler" with neurological actions in the mouse (Mus musculus L.). J Genet 1951;50:192-201
    • (1951) J Genet , vol.50 , pp. 192-201
    • Falconer, D.S.1
  • 17
    • 0024518749 scopus 로고
    • A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and humans
    • Buchberg AM, Brownell E, Nagata S, Jenkins NA, Copeland NG. A comprehensive genetic map of murine chromosome 11 reveals extensive linkage conservation between mouse and humans. Genetics 1989;122:153-161
    • (1989) Genetics , vol.122 , pp. 153-161
    • Buchberg, A.M.1    Brownell, E.2    Nagata, S.3    Jenkins, N.A.4    Copeland, N.G.5
  • 20
    • 0025942098 scopus 로고
    • Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene
    • Spreyer P, Kuhn G, Hanemann CO, Gillen C, Schaal H, Kuhn R, et al. Axon-regulated expression of a Schwann cell transcript that is homologous to a 'growth arrest-specific' gene. Embo J 1991;10:3661-3668
    • (1991) Embo J , vol.10 , pp. 3661-3668
    • Spreyer, P.1    Kuhn, G.2    Hanemann, C.O.3    Gillen, C.4    Schaal, H.5    Kuhn, R.6
  • 22
    • 0026879838 scopus 로고
    • Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A
    • Matsunami N, Smith B, Ballard L, Lensch MW, Robertson M, Albertsen H, et al. Peripheral myelin protein-22 gene maps in the duplication in chromosome 17p11.2 associated with Charcot-Marie-Tooth 1A. Nat Genet 1992;1:176-179
    • (1992) Nat Genet , vol.1 , pp. 176-179
    • Matsunami, N.1    Smith, B.2    Ballard, L.3    Lensch, M.W.4    Robertson, M.5    Albertsen, H.6
  • 23
    • 0026879614 scopus 로고
    • The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A
    • Patel PI, Roa BB, Welcher AA, Schoener-Scott R, Trask BJ, Pentao L, et al. The gene for the peripheral myelin protein PMP-22 is a candidate for Charcot-Marie-Tooth disease type 1A. Nat Genet 1992;1:159-165
    • (1992) Nat Genet , vol.1 , pp. 159-165
    • Patel, P.I.1    Roa, B.B.2    Welcher, A.A.3    Schoener-Scott, R.4    Trask, B.J.5    Pentao, L.6
  • 24
    • 0026879615 scopus 로고
    • The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication
    • Timmerman V, Nelis E, Van Hul W, Nieuwenhuijsen BW, Chen KL, Wang S, et al. The peripheral myelin protein gene PMP-22 is contained within the Charcot-Marie-Tooth disease type 1A duplication. Nat Genet 1992;1:171-175
    • (1992) Nat Genet , vol.1 , pp. 171-175
    • Timmerman, V.1    Nelis, E.2    Van Hul, W.3    Nieuwenhuijsen, B.W.4    Chen, K.L.5    Wang, S.6
  • 26
    • 0026519132 scopus 로고
    • Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)
    • Snipes GJ, Suter U, Welcher AA, Shooter EM. Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13). J Cell Biol 1992;117:225-238
    • (1992) J Cell Biol , vol.117 , pp. 225-238
    • Snipes, G.J.1    Suter, U.2    Welcher, A.A.3    Shooter, E.M.4
  • 27
    • 0028073907 scopus 로고
    • Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters
    • Suter U, Snipes GJ, Schoener-Scott R, Welcher AA, Pareek S, Lupski JR, et al. Regulation of tissue-specific expression of alternative peripheral myelin protein-22 (PMP22) gene transcripts by two promoters. J Biol Chem 1994;269;25795-25808
    • (1994) J Biol Chem , vol.269 , pp. 25795-25808
    • Suter, U.1    Snipes, G.J.2    Schoener-Scott, R.3    Welcher, A.A.4    Pareek, S.5    Lupski, J.R.6
  • 28
    • 0028221758 scopus 로고
    • Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A
    • Yoshikawa H, Nishimura T, Nakatsuji Y, Fujimura H, Himoro M, Hayasaka K, et al. Elevated expression of messenger RNA for peripheral myelin protein 22 in biopsied peripheral nerves of patients with Charcot-Marie-Tooth disease type 1A. Ann Neurol 1994;35:445-450
    • (1994) Ann Neurol , vol.35 , pp. 445-450
    • Yoshikawa, H.1    Nishimura, T.2    Nakatsuji, Y.3    Fujimura, H.4    Himoro, M.5    Hayasaka, K.6
  • 29
    • 0031471867 scopus 로고    scopus 로고
    • Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies
    • Gabriel JM, Erne B, Pareyson D, Sghirlanzoni A, Taroni F, Steck AJ. Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies. Neurology 1997; 49:1635-1640
    • (1997) Neurology , vol.49 , pp. 1635-1640
    • Gabriel, J.M.1    Erne, B.2    Pareyson, D.3    Sghirlanzoni, A.4    Taroni, F.5    Steck, A.J.6
  • 31
    • 0027314668 scopus 로고
    • Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene
    • Roa BB, Garcia CA, Suter U, Kulpa DA, Wise CA, Mueller J, et al. Charcot-Marie-Tooth disease type 1A. Association with a spontaneous point mutation in the PMP22 gene. New Engl J Med 1993;329:96-101
    • (1993) New Engl J Med , vol.329 , pp. 96-101
    • Roa, B.B.1    Garcia, C.A.2    Suter, U.3    Kulpa, D.A.4    Wise, C.A.5    Mueller, J.6
  • 32
    • 0030012076 scopus 로고    scopus 로고
    • A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease
    • Navon R, Seifried B, Gal-On NS, Sadeh M. A new point mutation affecting the fourth transmembrane domain of PMP22 results in severe de novo Charcot-Marie-Tooth disease. Hum Genet 1996;97:685-687
    • (1996) Hum Genet , vol.97 , pp. 685-687
    • Navon, R.1    Seifried, B.2    Gal-On, N.S.3    Sadeh, M.4
  • 34
    • 0027374931 scopus 로고
    • Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication
    • Wise CA, Garcia CA, Davis SN, Heju Z, Pentao L, Patel PI, et al. Molecular analyses of unrelated Charcot-Marie-Tooth (CMT) disease patients suggest a high frequency of the CMTIA duplication. Am J Hum Genet 1993;53:853-863
    • (1993) Am J Hum Genet , vol.53 , pp. 853-863
    • Wise, C.A.1    Garcia, C.A.2    Davis, S.N.3    Heju, Z.4    Pentao, L.5    Patel, P.I.6
  • 35
    • 0004074947 scopus 로고
    • Linkage of dominantly inherited Charcot-Marie-Tooth neuropathy to the Duffy locus in an Indian family
    • Stebbins NB, Conneally PM. Linkage of dominantly inherited Charcot-Marie-Tooth neuropathy to the Duffy locus in an Indian family. Am J Hum Genet 1982;34:388-394
    • (1982) Am J Hum Genet , vol.34 , pp. 388-394
    • Stebbins, N.B.1    Conneally, P.M.2
  • 36
    • 0025833803 scopus 로고
    • Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin
    • Hayasaka K, Nanao K, Tahara M, Sato W, Takada G, Miura M, et al. Isolation and sequence determination of cDNA encoding the major structural protein of human peripheral myelin. Biochem Biophys Res Commun 1991;180:515-518
    • (1991) Biochem Biophys Res Commun , vol.180 , pp. 515-518
    • Hayasaka, K.1    Nanao, K.2    Tahara, M.3    Sato, W.4    Takada, G.5    Miura, M.6
  • 37
    • 0027221141 scopus 로고
    • Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene
    • Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, et al. Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene. Nat Genet 1993;5:31-34
    • (1993) Nat Genet , vol.5 , pp. 31-34
    • Hayasaka, K.1    Himoro, M.2    Sato, W.3    Takada, G.4    Uyemura, K.5    Shimizu, N.6
  • 38
    • 0027221142 scopus 로고
    • Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B
    • Kulkens T, Bolhuis PA, Wolterman RA, Kemp S, te Nijenhuis S, Valentijn LJ, et al. Deletion of the serine 34 codon from the major peripheral myelin protein P0 gene in Charcot-Marie-Tooth disease type 1B. Nat Genet 1993;5:35-39
    • (1993) Nat Genet , vol.5 , pp. 35-39
    • Kulkens, T.1    Bolhuis, P.A.2    Wolterman, R.A.3    Kemp, S.4    Te Nijenhuis, S.5    Valentijn, L.J.6
  • 39
    • 0027338081 scopus 로고
    • Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B
    • Hayasaka K, Takada G, Ionasescu VV. Mutation of the myelin P0 gene in Charcot-Marie-Tooth neuropathy type 1B. Hum Mol Genet 1993;2:1369-1372
    • (1993) Hum Mol Genet , vol.2 , pp. 1369-1372
    • Hayasaka, K.1    Takada, G.2    Ionasescu, V.V.3
  • 41
    • 16044362374 scopus 로고    scopus 로고
    • Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination
    • Warner LE, Hilz MJ, Appel SH, Killian JM, Kolodry EH, Karpati G, et al. Clinical phenotypes of different MPZ (P0) mutations may include Charcot-Marie-Tooth type 1B, Dejerine-Sottas, and congenital hypomyelination. Neuron 1996;17:451-460
    • (1996) Neuron , vol.17 , pp. 451-460
    • Warner, L.E.1    Hilz, M.J.2    Appel, S.H.3    Killian, J.M.4    Kolodry, E.H.5    Karpati, G.6
  • 42
    • 0030048089 scopus 로고    scopus 로고
    • Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease
    • Roa BB, Warner LE, Garcia CA, Russo D, Lovelace R, Chance PF, et al. Myelin protein zero (MPZ) gene mutations in nonduplication type 1 Charcot-Marie-Tooth disease. Hum Mutat 1996;7:36-45
    • (1996) Hum Mutat , vol.7 , pp. 36-45
    • Roa, B.B.1    Warner, L.E.2    Garcia, C.A.3    Russo, D.4    Lovelace, R.5    Chance, P.F.6
  • 44
    • 0028131591 scopus 로고
    • Rapid screening of myelin genes in CMT1 patients by SSCP analysis: Identification of new mutations and polymorphisms in the P0 gene
    • Nelis E, Timmerman V, De Jonghe P, Vandenberghe A, Pham-Dinh D, Dautigny A, et al. Rapid screening of myelin genes in CMT1 patients by SSCP analysis: Identification of new mutations and polymorphisms in the P0 gene. Hum Genet 1994; 94:653-657
    • (1994) Hum Genet , vol.94 , pp. 653-657
    • Nelis, E.1    Timmerman, V.2    De Jonghe, P.3    Vandenberghe, A.4    Pham-Dinh, D.5    Dautigny, A.6
  • 45
    • 0027584197 scopus 로고
    • The molecular genetics of myelination: An update
    • Lemke G. The molecular genetics of myelination: An update. Glia 1993;7:263-271
    • (1993) Glia , vol.7 , pp. 263-271
    • Lemke, G.1
  • 46
    • 0027486810 scopus 로고
    • Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene
    • Roa BB, Dyck PJ, Marks HG, Chance PF, Lupski JR. Dejerine-Sottas syndrome associated with point mutation in the peripheral myelin protein 22 (PMP22) gene. Nat Genet 1993; 5:269-273
    • (1993) Nat Genet , vol.5 , pp. 269-273
    • Roa, B.B.1    Dyck, P.J.2    Marks, H.G.3    Chance, P.F.4    Lupski, J.R.5
  • 47
    • 0027422165 scopus 로고
    • De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III)
    • Hayasaka K, Himoro M, Sawaishi Y, Nanao K, Takahashi T, Takada G, et al. De novo mutation of the myelin P0 gene in Dejerine-Sottas disease (hereditary motor and sensory neuropathy type III). Nat Genet 1993;5:266-268
    • (1993) Nat Genet , vol.5 , pp. 266-268
    • Hayasaka, K.1    Himoro, M.2    Sawaishi, Y.3    Nanao, K.4    Takahashi, T.5    Takada, G.6
  • 48
    • 0032472256 scopus 로고    scopus 로고
    • Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome
    • Stogbauer F, Young P, Wiebusch H, Timmerman V, Kuhlenbaumer G, Nelis E, et al. Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndrome. Neurosci Lett 1998;240:1-4
    • (1998) Neurosci Lett , vol.240 , pp. 1-4
    • Stogbauer, F.1    Young, P.2    Wiebusch, H.3    Timmerman, V.4    Kuhlenbaumer, G.5    Nelis, E.6
  • 49
    • 0029153896 scopus 로고
    • Hereditary neuropathy with liability to pressure palsies and inherited brachial plexus neuropathy - Two genetically distinct disorders
    • Windebank AJ, Schenone A, Dewald GW. Hereditary neuropathy with liability to pressure palsies and inherited brachial plexus neuropathy - two genetically distinct disorders. Mayo Clin Proc 1995;70:743-746
    • (1995) Mayo Clin Proc , vol.70 , pp. 743-746
    • Windebank, A.J.1    Schenone, A.2    Dewald, G.W.3
  • 50
    • 0019494495 scopus 로고
    • Intensive evaluation of referred unclassified neuropathies yields improved diagnosis
    • Dyck PJ, Oviatt KF, Lambert EH. Intensive evaluation of referred unclassified neuropathies yields improved diagnosis. Ann Neurol 1981;10:222-226
    • (1981) Ann Neurol , vol.10 , pp. 222-226
    • Dyck, P.J.1    Oviatt, K.F.2    Lambert, E.H.3
  • 51
    • 0000325399 scopus 로고
    • The pathology of neuropathies with focal thickening of the myelin sheath (tomaculous neuropathy): Studies on the formation of the abnormal myelin sheath
    • Madrid R, Bradley WG. The pathology of neuropathies with focal thickening of the myelin sheath (tomaculous neuropathy): Studies on the formation of the abnormal myelin sheath. J Neurol Sci 1975;25:415-448
    • (1975) J Neurol Sci , vol.25 , pp. 415-448
    • Madrid, R.1    Bradley, W.G.2
  • 52
    • 0027509953 scopus 로고
    • DNA deletion associated with hereditary neuropathy with liability to pressure palsies
    • Chance PF, Alderson MK, Leppig KA, Lensch MW, Matsunami N, Smith B, et al. DNA deletion associated with hereditary neuropathy with liability to pressure palsies. Cell 1993;72: 143-151
    • (1993) Cell , vol.72 , pp. 143-151
    • Chance, P.F.1    Alderson, M.K.2    Leppig, K.A.3    Lensch, M.W.4    Matsunami, N.5    Smith, B.6
  • 53
    • 0027305348 scopus 로고
    • Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1
    • Mariman EC, Gabreels-Festen AA, van Beersum SE, Jongen PJ, Ropers HH, Gabreels FJ. Gene for hereditary neuropathy with liability to pressure palsies (HNPP) maps to chromosome 17 at or close to the locus for HMSN type 1. Hum Genet 1993;92: 87-90
    • (1993) Hum Genet , vol.92 , pp. 87-90
    • Mariman, E.C.1    Gabreels-Festen, A.A.2    Van Beersum, S.E.3    Jongen, P.J.4    Ropers, H.H.5    Gabreels, F.J.6
  • 54
    • 0027976968 scopus 로고
    • Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)
    • Le Guern E, Sturtz F, Gugenheim M, Gouider R, Bonnebouche C, Ravise N, et al. Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP). Cytogenet Cell Genet 1994;65: 261-264
    • (1994) Cytogenet Cell Genet , vol.65 , pp. 261-264
    • Le Guern, E.1    Sturtz, F.2    Gugenheim, M.3    Gouider, R.4    Bonnebouche, C.5    Ravise, N.6
  • 55
    • 0031441542 scopus 로고    scopus 로고
    • Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies
    • Schenone A, Nobbio L, Caponnetto C, Abbruzzese M, Mandich P, Bellone E, et al. Correlation between PMP-22 messenger RNA expression and phenotype in hereditary neuropathy with liability to pressure palsies. Ann Neurol 1997;42:866-872
    • (1997) Ann Neurol , vol.42 , pp. 866-872
    • Schenone, A.1    Nobbio, L.2    Caponnetto, C.3    Abbruzzese, M.4    Mandich, P.5    Bellone, E.6
  • 57
    • 0027972378 scopus 로고
    • Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
    • Chance PF, Abbas N, Lensch MW, Pentao L, Roa BB, Patel PI, et al. Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17. Hum Mol Genet 1994;3:223-228
    • (1994) Hum Mol Genet , vol.3 , pp. 223-228
    • Chance, P.F.1    Abbas, N.2    Lensch, M.W.3    Pentao, L.4    Roa, B.B.5    Patel, P.I.6
  • 59
    • 6844239521 scopus 로고    scopus 로고
    • Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination
    • Lopes J, Ravise N, Vandenberghe A, Palau F, Ionasescu V, Mayer M, et al. Fine mapping of de novo CMT1A and HNPP rearrangements within CMT1A-REPs evidences two distinct sex-dependent mechanisms and candidate sequences involved in recombination. Hum Mol Genet 1998;7:141-148
    • (1998) Hum Mol Genet , vol.7 , pp. 141-148
    • Lopes, J.1    Ravise, N.2    Vandenberghe, A.3    Palau, F.4    Ionasescu, V.5    Mayer, M.6
  • 60
    • 0029999248 scopus 로고    scopus 로고
    • Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot
    • Kiyosawa H, Chance PF. Primate origin of the CMT1A-REP repeat and analysis of a putative transposon-associated recombinational hotspot. Hum Mol Genet 1996;5:745-753
    • (1996) Hum Mol Genet , vol.5 , pp. 745-753
    • Kiyosawa, H.1    Chance, P.F.2
  • 61
    • 0030871024 scopus 로고    scopus 로고
    • The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs
    • Reiter LT, Murakami T, Koeuth T, Gibbs RA, Lupski JR. The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs. Hum Mol Genet 1997;6:1595-1603
    • (1997) Hum Mol Genet , vol.6 , pp. 1595-1603
    • Reiter, L.T.1    Murakami, T.2    Koeuth, T.3    Gibbs, R.A.4    Lupski, J.R.5
  • 62
    • 0029962292 scopus 로고    scopus 로고
    • A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element
    • Reiter LT, Murakami T, Koeuth T, Pentao L, Munzy DM, Gibbs RA, et al. A recombination hotspot responsible for two inherited peripheral neuropathies is located near a mariner transposon-like element. Nat Genet 1996;12:288-297
    • (1996) Nat Genet , vol.12 , pp. 288-297
    • Reiter, L.T.1    Murakami, T.2    Koeuth, T.3    Pentao, L.4    Munzy, D.M.5    Gibbs, R.A.6
  • 63
    • 0029989649 scopus 로고    scopus 로고
    • A Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: New tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group
    • Lopes J, LeGuern E, Gouider R, Tardieu S, Abbas N, Birouk N, et al. A Recombination hot spot in a 3.2-kb region of the Charcot-Marie-Tooth type 1A repeat sequences: New tools for molecular diagnosis of hereditary neuropathy with liability to pressure palsies and of Charcot-Marie-Tooth type 1A. French CMT Collaborative Research Group. Am J Hum Genet 1996;58:1223-1230
    • (1996) Am J Hum Genet , vol.58 , pp. 1223-1230
    • Lopes, J.1    Leguern, E.2    Gouider, R.3    Tardieu, S.4    Abbas, N.5    Birouk, N.6
  • 64
    • 17144461625 scopus 로고    scopus 로고
    • Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP
    • Yamamoto M, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, Yanagihara T, et al. Locations of crossover breakpoints within the CMT1A-REP repeat in Japanese patients with CMT1A and HNPP. Hum Genet 1997;99:151-154
    • (1997) Hum Genet , vol.99 , pp. 151-154
    • Yamamoto, M.1    Yasuda, T.2    Hayasaka, K.3    Ohnishi, A.4    Yoshikawa, H.5    Yanagihara, T.6
  • 65
    • 16944365439 scopus 로고    scopus 로고
    • Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent
    • Timmerman V, Rautenstrauss B, Reiter LT, Koeuth T, Lofgren A, Liehr T, et al. Detection of the CMT1A/HNPP recombination hotspot in unrelated patients of European descent. J Med Genet 1997;34:43-49
    • (1997) J Med Genet , vol.34 , pp. 43-49
    • Timmerman, V.1    Rautenstrauss, B.2    Reiter, L.T.3    Koeuth, T.4    Lofgren, A.5    Liehr, T.6
  • 66
    • 6844249444 scopus 로고    scopus 로고
    • Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeat
    • Yamamoto M, Keller MP, Yasuda T, Hayasaka K, Ohnishi A, Yoshikawa H, et al. Clustering of CMT1A duplication breakpoints in a 700 bp interval of the CMT1A-REP repeat. Hum Mutat 1998;11:109-113
    • (1998) Hum Mutat , vol.11 , pp. 109-113
    • Yamamoto, M.1    Keller, M.P.2    Yasuda, T.3    Hayasaka, K.4    Ohnishi, A.5    Yoshikawa, H.6
  • 67
    • 0031972093 scopus 로고    scopus 로고
    • Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients
    • Reiter LT, Hastings PJ, Nelis E, De Jonghe P, Van Broeckhoven C, Lupski JR. Human meiotic recombination products revealed by sequencing a hotspot for homologous strand exchange in multiple HNPP deletion patients. Am J Hum Genet 1998;62:1023-1033
    • (1998) Am J Hum Genet , vol.62 , pp. 1023-1033
    • Reiter, L.T.1    Hastings, P.J.2    Nelis, E.3    De Jonghe, P.4    Van Broeckhoven, C.5    Lupski, J.R.6
  • 68
    • 0028810444 scopus 로고
    • Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP
    • Kiyosawa H, Lensch MW, Chance PF. Analysis of the CMT1A-REP repeat: Mapping crossover breakpoints in CMT1A and HNPP. Hum Mol Genet 1995;4:2327-2334
    • (1995) Hum Mol Genet , vol.4 , pp. 2327-2334
    • Kiyosawa, H.1    Lensch, M.W.2    Chance, P.F.3
  • 69
    • 0031573383 scopus 로고    scopus 로고
    • The Charcot-Marie-Tooth binary repeat contains a gene transcribed from the opposite strand of a partially duplicated region of the COX10 gene
    • Kennerson ML, Nassif NT, Dawkins JL, DeKroon RM, Yang JG, Nicholson GA. The Charcot-Marie-Tooth binary repeat contains a gene transcribed from the opposite strand of a partially duplicated region of the COX10 gene. Genomics 1997;46:61-69
    • (1997) Genomics , vol.46 , pp. 61-69
    • Kennerson, M.L.1    Nassif, N.T.2    Dawkins, J.L.3    Dekroon, R.M.4    Yang, J.G.5    Nicholson, G.A.6
  • 70
    • 0018949405 scopus 로고
    • Genetic aspects of hereditary motor and sensory neuropathy (types I and II)
    • Harding AE, Thomas PK. Genetic aspects of hereditary motor and sensory neuropathy (types I and II). J Med Genet 1980;17:329-336
    • (1980) J Med Genet , vol.17 , pp. 329-336
    • Harding, A.E.1    Thomas, P.K.2
  • 71
    • 0027317609 scopus 로고
    • Localization of a gene (CMT2A) for autosomal dom nant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
    • Ben Othmane K, Middleton LT, Loprest LJ, Wilkinson KM, Lennon F, Rozear MP, et al. Localization of a gene (CMT2A) for autosomal dom nant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. Genomics 1993;17:370-375
    • (1993) Genomics , vol.17 , pp. 370-375
    • Ben Othmane, K.1    Middleton, L.T.2    Loprest, L.J.3    Wilkinson, K.M.4    Lennon, F.5    Rozear, M.P.6
  • 72
    • 0031470266 scopus 로고    scopus 로고
    • Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A
    • Saito M, Hayashi Y, Suzuki T, Tanaka H, Hozumi I, Tsuji S. Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A. Neurology 1997;49:1630-1635
    • (1997) Neurology , vol.49 , pp. 1630-1635
    • Saito, M.1    Hayashi, Y.2    Suzuki, T.3    Tanaka, H.4    Hozumi, I.5    Tsuji, S.6
  • 75
    • 0030011973 scopus 로고    scopus 로고
    • Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2
    • Yoshioka R, Dyck PJ, Chance PF. Genetic heterogeneity in Charcot-Marie-Tooth neuropathy type 2. Neurology 1996;46: 569-571
    • (1996) Neurology , vol.46 , pp. 569-571
    • Yoshioka, R.1    Dyck, P.J.2    Chance, P.F.3
  • 77
    • 0029894937 scopus 로고    scopus 로고
    • Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13
    • Timmerman V, De Jonghe P, Spoelders P, Simokovic S, Lofgren A, Nelis E, et al. Linkage and mutation analysis of Charcot-Marie-Tooth neuropathy type 2 families with chromosomes 1p35-p36 and Xq13. Neurology 1996;46:1311-1318
    • (1996) Neurology , vol.46 , pp. 1311-1318
    • Timmerman, V.1    De Jonghe, P.2    Spoelders, P.3    Simokovic, S.4    Lofgren, A.5    Nelis, E.6
  • 78
    • 0005046359 scopus 로고
    • Relation of hereditary pattern to clinical severity as illustrated by peroneal atrophy
    • Allan W. Relation of hereditary pattern to clinical severity as illustrated by peroneal atrophy. Arch Intern Med 1939;63:1123-1131
    • (1939) Arch Intern Med , vol.63 , pp. 1123-1131
    • Allan, W.1
  • 79
    • 0018962193 scopus 로고
    • Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial clinical manifestations in female carriers
    • Fryns JP, Van den Berghe H. Sex-linked recessive inheritance in Charcot-Marie-Tooth disease with partial clinical manifestations in female carriers. Hum Genet 1980;55:413-415
    • (1980) Hum Genet , vol.55 , pp. 413-415
    • Fryns, J.P.1    Van Den Berghe, H.2
  • 80
    • 0021908106 scopus 로고
    • X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal Xq
    • Gal A, Mucke J, Theile H, Wieacker PF, Ropers HH, Wienker TF. X-linked dominant Charcot-Marie-Tooth disease: Suggestion of linkage with a cloned DNA sequence from the proximal Xq. Hum Genet 1985;70:38-42
    • (1985) Hum Genet , vol.70 , pp. 38-42
    • Gal, A.1    Mucke, J.2    Theile, H.3    Wieacker, P.F.4    Ropers, H.H.5    Wienker, T.F.6
  • 83
    • 0025731521 scopus 로고
    • X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region
    • Mostacciuolo ML, Muller E, Fardin P, Micaglio GF, Bardoni B, Guioli S, et al. X-linked Charcot-Marie-Tooth disease. A linkage study in a large family by using 12 probes of the pericentromeric region. Hum Genet 1991;87:23-27
    • (1991) Hum Genet , vol.87 , pp. 23-27
    • Mostacciuolo, M.L.1    Muller, E.2    Fardin, P.3    Micaglio, G.F.4    Bardoni, B.5    Guioli, S.6
  • 86
    • 0028082335 scopus 로고
    • Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy
    • Fain PR, Barker DF, Chance PF. Refined genetic mapping of X-linked Charcot-Marie-Tooth neuropathy. Am J Hum Genet 1994;54:229-235
    • (1994) Am J Hum Genet , vol.54 , pp. 229-235
    • Fain, P.R.1    Barker, D.F.2    Chance, P.F.3
  • 88
    • 0029014126 scopus 로고
    • Molecular anatomy and genetics of myelin proteins in the peripheral nervous system
    • Snipes GJ, Suter U. Molecular anatomy and genetics of myelin proteins in the peripheral nervous system. J Anat 1995;186: 483-494
    • (1995) J Anat , vol.186 , pp. 483-494
    • Snipes, G.J.1    Suter, U.2
  • 90
    • 0028088839 scopus 로고
    • Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy
    • Ionasescu V, Searby C, Ionasescu R. Point mutations of the connexin32 (GJB1) gene in X-linked dominant Charcot-Marie-Tooth neuropathy. Hum Mol Genet 1994;3:355-358
    • (1994) Hum Mol Genet , vol.3 , pp. 355-358
    • Ionasescu, V.1    Searby, C.2    Ionasescu, R.3
  • 91
    • 0029788204 scopus 로고    scopus 로고
    • Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy
    • Ionasescu VV, Searby C, Ionsasescu R, Neuhaus IM, Werner R. Mutations of the noncoding region of the connexin32 gene in X-linked dominant Charcot-Marie-Tooth neuropathy. Neurology 1996;47:541-544
    • (1996) Neurology , vol.47 , pp. 541-544
    • Ionasescu, V.V.1    Searby, C.2    Ionsasescu, R.3    Neuhaus, I.M.4    Werner, R.5
  • 94
    • 0032518241 scopus 로고    scopus 로고
    • Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression
    • Yoshimura T, Sataka M, Ohnishi A, Tsutsumi Y, Fujikura Y. Mutations of connexin32 in Charcot-Marie-Tooth disease type X interfere with cell-to-cell communication but not cell proliferation and myelin-specific gene expression. J Neurosci Res 1998;51:154-161
    • (1998) J Neurosci Res , vol.51 , pp. 154-161
    • Yoshimura, T.1    Sataka, M.2    Ohnishi, A.3    Tsutsumi, Y.4    Fujikura, Y.5
  • 95
    • 0031943222 scopus 로고    scopus 로고
    • Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies
    • Warner LE, Mancias P, Butler IJ, McDonald CM, Keppen L, Koob KG, et al. Mutations in the early growth response 2 (EGR2) gene are associated with hereditary myelinopathies. Nat Genet 1998;18:382-384
    • (1998) Nat Genet , vol.18 , pp. 382-384
    • Warner, L.E.1    Mancias, P.2    Butler, I.J.3    McDonald, C.M.4    Keppen, L.5    Koob, K.G.6
  • 96
    • 0030221510 scopus 로고    scopus 로고
    • The Transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation
    • Zorick TS, Syroid DE, Arroyo E, Scherer SS, Lemke G. The Transcription factors SCIP and Krox-20 mark distinct stages and cell fates in Schwann cell differentiation. Mol Cell Neurosci 1996;8:129-145
    • (1996) Mol Cell Neurosci , vol.8 , pp. 129-145
    • Zorick, T.S.1    Syroid, D.E.2    Arroyo, E.3    Scherer, S.S.4    Lemke, G.5
  • 97
    • 0027491703 scopus 로고
    • Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q
    • Ben Othmane K, Hentati F, Lennon F, Ben Hamida C, Blel S, Roses AD, et al. Linkage of a locus (CMT4A) for autosomal recessive Charcot-Marie-Tooth disease to chromosome 8q. Hum Mol Genet 1993;2:1625-1628
    • (1993) Hum Mol Genet , vol.2 , pp. 1625-1628
    • Ben Othmane, K.1    Hentati, F.2    Lennon, F.3    Ben Hamida, C.4    Blel, S.5    Roses, A.D.6
  • 98
    • 0029128280 scopus 로고
    • Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A
    • Ben Othmane KB, Loeb D, Hayworth-Hodgte R, Hentati F, Rao N, Roses A, et al. Physical and genetic mapping of the CMT4A locus and exclusion of PMP-2 as the defect in CMT4A. Genomics 1995;28:286-290
    • (1995) Genomics , vol.28 , pp. 286-290
    • Ben Othmane, K.B.1    Loeb, D.2    Hayworth-Hodgte, R.3    Hentati, F.4    Rao, N.5    Roses, A.6
  • 99
    • 0030015647 scopus 로고    scopus 로고
    • Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing
    • Bolino A, Brancolini V, Bono F, Bruni A, Gambardella A, Romeo G, et al. Localization of a gene responsible for autosomal recessive demyelinating neuropathy with focally folded myelin sheaths to chromosome 11q23 by homozygosity mapping and haplotype sharing. Hum Mol Genet 1996;5:1051-1054
    • (1996) Hum Mol Genet , vol.5 , pp. 1051-1054
    • Bolino, A.1    Brancolini, V.2    Bono, F.3    Bruni, A.4    Gambardella, A.5    Romeo, G.6
  • 100
    • 0031942903 scopus 로고    scopus 로고
    • Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B)
    • Gambardella A, Bolino A, Muglia M, Valentino P, Bono F, Oliveri RL, et al. Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths (CMT4B). Neurology 1998;50:799-801
    • (1998) Neurology , vol.50 , pp. 799-801
    • Gambardella, A.1    Bolino, A.2    Muglia, M.3    Valentino, P.4    Bono, F.5    Oliveri, R.L.6
  • 101
    • 0000751211 scopus 로고
    • Hereditary sensory radicular neuropathy
    • Denny-Brown D. Hereditary sensory radicular neuropathy. J Neurol Neurosurg Psychiatry 1951;14:237-252
    • (1951) J Neurol Neurosurg Psychiatry , vol.14 , pp. 237-252
    • Denny-Brown, D.1
  • 102
    • 0030704747 scopus 로고    scopus 로고
    • Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1 ;raq22.3: Exclusion of GAS1 and XPA
    • Blair IP, Dawkins JL, Nicholson GA. Fine mapping of the hereditary sensory neuropathy type I locus on chromosome 9q22.1 ;raq22.3: Exclusion of GAS1 and XPA. Cytogenet Cell Genet 1997;78:140-144
    • (1997) Cytogenet Cell Genet , vol.78 , pp. 140-144
    • Blair, I.P.1    Dawkins, J.L.2    Nicholson, G.A.3
  • 103
    • 0025892749 scopus 로고
    • Penetrance of the hereditary motor and sensory neuropathy Ia mutation: Assessment by nerve conduction studies
    • Nicholson GA. Penetrance of the hereditary motor and sensory neuropathy Ia mutation: Assessment by nerve conduction studies. Neurology 1991;41:547-552
    • (1991) Neurology , vol.41 , pp. 547-552
    • Nicholson, G.A.1
  • 104
    • 0028847995 scopus 로고
    • Charcot-Marie-Tooth neuropathies: From clinical description to molecular genetics
    • Ionasescu VV. Charcot-Marie-Tooth neuropathies: From clinical description to molecular genetics. Muscle Nerve 1995;18: 267-275
    • (1995) Muscle Nerve , vol.18 , pp. 267-275
    • Ionasescu, V.V.1
  • 105
    • 0028950408 scopus 로고
    • Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth
    • Zoidl G, Blass-Kampmann S, D'Urso D, Schmalenbach C, Muller HW. Retroviral-mediated gene transfer of the peripheral myelin protein PMP22 in Schwann cells: Modulation of cell growth. Embo J 1995;14:1122-1128
    • (1995) Embo J , vol.14 , pp. 1122-1128
    • Zoidl, G.1    Blass-Kampmann, S.2    D'Urso, D.3    Schmalenbach, C.4    Muller, H.W.5
  • 106
    • 0028784820 scopus 로고
    • Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
    • Adlkofer K, Martini R, Aguzzi A, Zielasek J, Toyka KV, Suter U. Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice. Nat Genet 1995;11:274-280
    • (1995) Nat Genet , vol.11 , pp. 274-280
    • Adlkofer, K.1    Martini, R.2    Aguzzi, A.3    Zielasek, J.4    Toyka, K.V.5    Suter, U.6
  • 107
    • 0032948050 scopus 로고    scopus 로고
    • Effects of PMP22 duplication and deletions on the axonal cytoskeleton
    • Sahenk Z, Chen L, Mendell JR. Effects of PMP22 duplication and deletions on the axonal cytoskeleton. Ann Neurol 1999; 45:16-24
    • (1999) Ann Neurol , vol.45 , pp. 16-24
    • Sahenk, Z.1    Chen, L.2    Mendell, J.R.3
  • 108
    • 0032894049 scopus 로고    scopus 로고
    • Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies
    • Naef R, Suter U. Impaired intracellular trafficking is a common disease mechanism of PMP22 point mutations in peripheral neuropathies. Neurobiol Dis 1999;6:1-14
    • (1999) Neurobiol Dis , vol.6 , pp. 1-14
    • Naef, R.1    Suter, U.2
  • 110
    • 0031044996 scopus 로고    scopus 로고
    • Connexins, gap junctions and cell-cell signalling in the nervous system
    • Bruzzone R, Ressot C. Connexins, gap junctions and cell-cell signalling in the nervous system. Eur J Neurosci 1997;9:1-6
    • (1997) Eur J Neurosci , vol.9 , pp. 1-6
    • Bruzzone, R.1    Ressot, C.2


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