Molecular and Functional Characterization of Novel Hypertrophic Cardiomyopathy Susceptibility Mutations in TNNC1- Encoded Troponin C

Hypertrophic Cardiomyopathy (HCM) is a common primary cardiac disorder defined by a hypertrophied left ventricle, is one of the main causes of sudden death in young athletes and has been associated with mutations in most sarcomeric proteins (tropomyosin, Troponin T and I, and actin, etc.). Many of t...

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Main Authors: Landstrom, Andrew P., Parvatiyar, Michelle S., Pinto, Jose R., Marquardt, Michelle L., Bos, J. Martijn, Tester, David J., Ommen, Steve R., Potter, James D., Ackerman, Michael J.
Formato: Artigo
Idioma:Inglês
Publicado em: 2008
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2627482/
https://ncbi.nlm.nih.gov/pubmed/18572189
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.yjmcc.2008.05.003
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