Detection of a new mutation in the beta-myosin heavy chain gene in an individual with hypertrophic cardiomyopathy.

Familial hypertrophic cardiomyopathy (FHCM) is an autosomal dominant disease affecting primarily the myocardium. The gene responsible for FHCM has been localized to chromosome 14 in some families and several mutations have been described in the beta-myosin heavy chain (beta MHC), a candidate gene fo...

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Bibliografske podrobnosti

izdano v:	J Clin Invest
Principais autores:	Marian, A J, Yu, Q T, Mares, A, Hill, R, Roberts, R, Perryman, M B
Format:	Artigo
Jezik:	Inglês
Izdano:	American Society for Clinical Investigation 1992
Teme:	Research Article
Online dostop:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443366/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1361491/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI116101
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