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Volumn 51, Issue 3, 2003, Pages 417-419

Merosin negative congenital muscular dystrophy: A short report

Author keywords

Congenital muscular dystrophy; Merosin deficiency

Indexed keywords

CREATINE KINASE; MEROSIN; MONOCLONAL ANTIBODY;

EID: 0348143404     PISSN: 00283886     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (5)

References (11)
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  • 3
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  • 5
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    • Localization of merosin negative congenital muscular dystrophy to chromosome 6q 2 by homozygosity mapping
    • Hillaire D, Leclerc A, Faure S, et al. Localization of merosin negative congenital muscular dystrophy to chromosome 6q 2 by homozygosity mapping. Hum Med Genet 1994;3:1657-61.
    • (1994) Hum Med Genet , vol.3 , pp. 1657-1661
    • Hillaire, D.1    Leclerc, A.2    Faure, S.3
  • 6
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    • Vachon, P.H.1    Loechel, F.2    Xu, H.3
  • 7
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    • (1997) Neuromusc Disord , vol.7 , pp. 169-175
    • Sewry, C.A.1    Naom, I.2    D'Alessandro, M.3
  • 8
    • 0028788685 scopus 로고
    • Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy
    • Shorer Z, Philpot J, Muntoni F, et al. Demyelinating peripheral neuropathy in merosin-deficient congenital muscular dystrophy. J Child Neurol 1995;10:472-5.
    • (1995) J Child Neurol , vol.10 , pp. 472-475
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  • 9
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    • Genetics of laminin alpha 2 chain (or merosin) deficient congenital muscular dystrophy: From identification of mutations to prenatal diagnosis
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  • 10
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    • Deficiency of merosin in dystrophic dy mice and genetic linkage of the laminin M chain gene to dy locus
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.