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...

Descrición completa

Detalles Bibliográficos

Publicado en:	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:	American Society for Clinical Investigation 1992
Assuntos:	Research Article
Acceso en liña:	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
Tags:	Engadir etiqueta Sen Etiquetas, Sexa o primeiro en etiquetar este rexistro!