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Inherited cardiomyopathies caused by troponin mutations

Genetic investigations of cardiomyopathy in the recent two decades have revealed a large number of mutations in the genes encoding sarcomeric proteins as a cause of inherited hypertrophic cardiomyopathy (HCM), dilated cardiomyopathy (DCM), or restrictive cardiomyopathy (RCM). Most functional analyse...

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Detalles Bibliográficos
Autores principales:	Lu, Qun-Wei, Wu, Xiao-Yan, Morimoto, Sachio
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Science Press 2013
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3627712/ https://www.ncbi.nlm.nih.gov/pubmed/23610579 http://dx.doi.org/10.3969/j.issn.1671-5411.2013.01.014

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