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...

Descripción completa

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

Internet

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

Ejemplares similares