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Muscle dysfunction in hypertrophic cardiomyopathy: What is needed to move to translation?
Hypertrophic cardiomyopathy (HCM) is caused by mutations in sarcomere genes. As such, HCM provides remarkable opportunities to study how changes to the heart’s molecular motor apparatus may influence cardiac structure and function. Although the genetic basis of HCM is well-described, there is much m...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3982612/ https://ncbi.nlm.nih.gov/pubmed/24493262 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10974-014-9374-0 |
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