Abnormal expression of laminin suggests disturbance of sarcolemma-extracellular matrix interaction in Japanese patients with autosomal recessive muscular dystrophy deficient in adhalin.

Dystrophin is associated with several novel sarcolemmal proteins, including a laminin-binding extracellular glycoprotein of 156 kD (alpha-dystroglycan) and a transmembrane glycoprotein of 50 kD (adhalin). Deficiency of adhalin characterizes a severe autosomal recessive muscular dystrophy prevalent i...

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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Higuchi, I, Yamada, H, Fukunaga, H, Iwaki, H, Okubo, R, Nakagawa, M, Osame, M, Roberds, S L, Shimizu, T, Campbell, K P
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1994
Assuntos:	Research Article
Acesso em linha:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC296136/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8040315/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI117375
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