Substitution of a conserved cysteine-996 in a cysteine-rich motif of the laminin α2-chain in congenital muscular dystrophy with partial deficiency of the protein

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Bibliographic Details
Published in:American journal of human genetics 1996, Vol.58 (6), p.1177-1184
Main Authors: NISSINEN, M, HELBLING-LECLERC, A, TRYGGVASON, K, GUICHENEY, P, ZHANG, X, EVANGELISTA, T, TOPALOGLU, H, CRUAUD, C, WEISSENBACH, J, FARDEAU, M, TOME, F. M. S, SCHWARTZ, K
Format: Article
Language:English
Subjects:
Biological and medical sciences
Diseases of striated muscles. Neuromuscular diseases
Medical sciences
Neurology
Online Access:Get full text
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ISSN:0002-9297
1537-6605