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Genetic mutations and mechanisms in dilated cardiomyopathy
Genetic mutations account for a significant percentage of cardiomyopathies, which are a leading cause of congestive heart failure. In hypertrophic cardiomyopathy (HCM), cardiac output is limited by the thickened myocardium through impaired filling and outflow. Mutations in the genes encoding the thi...
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| Main Authors: | , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
American Society for Clinical Investigation
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3533274/ https://ncbi.nlm.nih.gov/pubmed/23281406 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI62862 |
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