Refinement of the laminin alpha2 chain locus to human chromosome 6q2 in severe and mild merosin deficient congenital muscular dystrophy.

About half of the children with classical congenital muscular dystrophy (CMD) show an absence in their skeletal muscle of laminin alpha2 chain, one of the components of the extracellular matrix protein, merosin. Linkage analysis implicated the laminin alpha2 chain gene (LAMA2) on chromosome 6q2, now...

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Main Authors: Naom, I S, D'Alessandro, M, Topaloglu, H, Sewry, C, Ferlini, A, Helbling-Leclerc, A, Guicheney, P, Weissenbach, J, Schwartz, K, Bushby, K, Philpot, J, Dubowitz, V, Muntoni, F
Formáid: Artigo
Teanga:Inglês
Foilsithe: 1997
Ábhair:
Research Article
Rochtain Ar Líne:https://ncbi.nlm.nih.gov/pmc/articles/PMC1050860/
https://ncbi.nlm.nih.gov/pubmed/9039983
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