Functional analyses of troponin T mutations that cause hypertrophic cardiomyopathy: Insights into disease pathogenesis and troponin function

Mutations in a number of cardiac sarcomeric protein genes cause hypertrophic cardiomyopathy (HCM). Previous findings indicate that HCM-causing mutations associated with a truncated cardiac troponin T (TnT) and missense mutations in the β-myosin heavy chain share abnormalities in common, acting as do...

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Pubblicato in:	Proc Natl Acad Sci U S A
Autori principali:	Sweeney, H. Lee, Feng, Huisheng S., Yang, Zhaouhui, Watkins, Hugh
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	National Academy of Sciences 1998
Soggetti:	Biological Sciences
Accesso online:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC24386/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/9826713/ https://ncbi.nlm.nih.govhttps://doi.org/10.1073/pnas.95.24.14406
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