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Skeletal muscle expression and abnormal function of beta-myosin in hypertrophic cardiomyopathy.

Hypertrophic cardiomyopathy is an important inherited disease. The phenotype has been linked, in some kindreds, to the beta-myosin heavy chain (beta-MHC) gene. Missense and silent mutations in the beta-MHC gene were used as markers to demonstrate the expression of mutant and normal cardiac beta-MHC...

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Bibliográfalaš dieđut
Publikašuvnnas:J Clin Invest
Váldodahkkit: Cuda, G, Fananapazir, L, Zhu, W S, Sellers, J R, Epstein, N D
Materiálatiipa: Artigo
Giella:Inglês
Almmustuhtton: American Society for Clinical Investigation 1993
Fáttát:
Liŋkkat:https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443355/
https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8514894/
https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116530
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