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Volumn 50, Issue 3, 1998, Pages 799-801

Genetic heterogeneity in autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin-sheaths (CMT4B)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; ARTICLE; CASE REPORT; CHROMOSOME 11Q; FEMALE; GENE MAPPING; GENETIC HETEROGENEITY; HAPLOTYPE; HEREDITARY MOTOR SENSORY NEUROPATHY; HUMAN; HUMAN CELL; MALE; MYELIN SHEATH; PEDIGREE; PRIORITY JOURNAL;

EID: 0031942903     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/WNL.50.3.799     Document Type: Article
Times cited : (42)

References (10)
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    • Gabreëls-Festen, A.1    Gabreëls, F.2
  • 2
    • 0030900182 scopus 로고    scopus 로고
    • A clinical, electrophysiologic, neuropathologic, and genetic study of two Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease
    • Kessali M, Zemmouri R, Guilbot A, et al. et al. A clinical, electrophysiologic, neuropathologic, and genetic study of two Algerian families with an autosomal recessive demyelinating form of Charcot-Marie-Tooth disease. Neurology 1997;48:867-873.
    • (1997) Neurology , vol.48 , pp. 867-873
    • Kessali, M.1    Zemmouri, R.2    Guilbot, A.3
  • 3
    • 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, 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
  • 4
    • 9344241377 scopus 로고    scopus 로고
    • Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. Clinical, elctrophysiologic, and genetic aspects of a large family
    • Quattrone A, Gambardella A, Bono F, et al. Autosomal recessive hereditary motor and sensory neuropathy with focally folded myelin sheaths. Clinical, elctrophysiologic, and genetic aspects of a large family. Neuorology 1996;46:1318-1324.
    • (1996) Neuorology , vol.46 , pp. 1318-1324
    • Quattrone, A.1    Gambardella, A.2    Bono, F.3
  • 5
    • 0029849358 scopus 로고    scopus 로고
    • Homozygosity mapiping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33
    • LeGuern E, Guilbot A, Kessali M, et al. Homozygosity mapiping of an autosomal recessive form of demyelinating Charcot-Marie-Tooth disease to chromosome 5q23-q33. Hum Mol Genet 1996;5:1685-1688.
    • (1996) Hum Mol Genet , vol.5 , pp. 1685-1688
    • LeGuern, E.1    Guilbot, A.2    Kessali, M.3
  • 6
    • 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, 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
  • 7
    • 0027317609 scopus 로고
    • Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity
    • Ben Othmane K, Middleton LT, Loprest LJ, et al. Localization of a gene (CMT2A) for autosomal dominant 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
  • 8
    • 0029150128 scopus 로고
    • Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q
    • Kwon JM, Elliott JL, Yee WC, et al. Assignment of a second Charcot-Marie-Tooth type II locus to chromosome 3q. Am J Hum Genet 1995;57:853-858.
    • (1995) Am J Hum Genet , vol.57 , pp. 853-858
    • Kwon, J.M.1    Elliott, J.L.2    Yee, W.C.3
  • 10
    • 0029058673 scopus 로고
    • From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myeloin protein
    • Harding AE. From the syndrome of Charcot, Marie and Tooth to disorders of peripheral myeloin protein. Brain 1995;118: 809-818.
    • (1995) Brain , vol.118 , pp. 809-818
    • Harding, A.E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.