Clinical implications of hypertrophic cardiomyopathy associated with mutations in the alpha-tropomyosin gene.

OBJECTIVE: The disease-bearing genes for hypertrophic cardiomyopathy (HCM) in HCM families have been identified as the beta-myosin heavy chain, alpha-tropomyosin, and cardiac troponin T genes. Three HCM kindreds with three distinct point mutations in the alpha-tropomyosin gene had extensive clinical...

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Detalhes bibliográficos
Main Authors: Yamauchi-Takihara, K., Nakajima-Taniguchi, C., Matsui, H., Fujio, Y., Kunisada, K., Nagata, S., Kishimoto, T.
Formato: Artigo
Idioma:Inglês
Publicado em: 1996
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC484428/
https://ncbi.nlm.nih.gov/pubmed/8774330
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