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Hypertrophic Cardiomyopathy: How do Mutations Lead to Disease?

Hypertrophic cardiomyopathy (HCM) is the most common monogenic genetic cardiac disease, with an estimated prevalence of 1:500 in the general population. Clinically, HCM is characterized by hypertrophy of the left ventricle (LV) walls, especially the septum, usually asymmetric, in the absence of any...

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Detalles Bibliográficos
Autores principales: Marsiglia, Júlia Daher Carneiro, Pereira, Alexandre Costa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3987320/
https://www.ncbi.nlm.nih.gov/pubmed/24714796
http://dx.doi.org/10.5935/abc.20140022