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The genetics of hypertrophic cardiomyopathy
Hypertrophic cardiomyopathy (HCM) is most commonly transmitted as an autosomal dominant trait, caused by mutations in genes encoding cardiac sarcomere proteins(1–3). Other inheritable causes of the disease include mutations in genes coding for proteins important in calcium handling or that form part...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Magdi Yacoub Heart Foundation
2018
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6209452/ https://www.ncbi.nlm.nih.gov/pubmed/30393648 http://dx.doi.org/10.21542/gcsp.2018.36 |