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Genetics of hypertrophic cardiomyopathy: advances and pitfalls in molecular diagnosis and therapy
Hypertrophic cardiomyopathy (HCM) is a primary disease of the cardiac muscle that occurs mainly due to mutations (>1,400 variants) in genes encoding for the cardiac sarcomere. HCM, the most common familial form of cardiomyopathy, affecting one in every 500 people in the general population, is typ...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Dove Medical Press
2014
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4199654/ https://www.ncbi.nlm.nih.gov/pubmed/25328416 http://dx.doi.org/10.2147/TACG.S49126 |