Altered cardiac troponin T in vitro function in the presence of a mutation implicated in familial hypertrophic cardiomyopathy.

Familial hypertrophic cardiomyopathy (HCM) can be caused by dominant missense mutations in cardiac troponin T (TnT), alpha-tropomyosin, C-protein, or cardiac myosin heavy chain genes. The myosin mutations are known to impair function, but any functional consequences of the TnT mutations are unknown....

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Publié dans:	J Clin Invest
Auteurs principaux:	Lin, D, Bobkova, A, Homsher, E, Tobacman, L S
Format:	Artigo
Langue:	Inglês
Publié:	American Society for Clinical Investigation 1996
Sujets:	Research Article
Accès en ligne:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC507378/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/8675696/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI118740
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