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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...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Sociedade Brasileira de Cardiologia
2014
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| 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 |