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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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Bibliografski detalji
Glavni autori: McNally, Elizabeth M., Golbus, Jessica R., Puckelwartz, Megan J.
Format: Artigo
Jezik:Inglês
Izdano: American Society for Clinical Investigation 2013
Teme:
Online pristup: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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