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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Detalhes bibliográficos

Publicado no:	J Clin Invest
Principais autores:	Marian, A J, Yu, Q T, Mares, A, Hill, R, Roberts, R, Perryman, M B
Formato:	Artigo
Idioma:	Inglês
Publicado em:	American Society for Clinical Investigation 1992
Assuntos:	Research Article
Acesso em linha:	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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