Human adhalin is alternatively spliced and the gene is located on chromosome 17q21.

Mutations in the dystrophin gene cause the X chromosome-linked, recessive Duchenne and Becker muscular dystrophies. Dystrophin, a large cytoskeletal protein, copurifies with a complex of dystrophin-associated proteins which serve to anchor dystrophin to the sarcolemma. One of these associated protei...

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Detalles Bibliográficos

Publicado en:	Proc Natl Acad Sci U S A
Principais autores:	McNally, E M, Yoshida, M, Mizuno, Y, Ozawa, E, Kunkel, L M
Formato:	Artigo
Idioma:	Inglês
Publicado:	National Academy of Sciences 1994
Assuntos:	Research Article
Acceso en liña:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC44882/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/7937874/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.91.21.9690
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