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MYBPC3's alternate ending: consequences and therapeutic implications of a highly prevalent 25 bp deletion mutation
Hypertrophic cardiomyopathy (HCM) is the most common form of inherited cardiac disease and the leading cause of sudden cardiac death in young people. HCM is caused by mutations in genes encoding contractile proteins. Cardiac myosin binding protein-C (cMyBP-C) is a thick filament contractile protein...
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| Main Authors: | , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3946836/ https://ncbi.nlm.nih.gov/pubmed/24327208 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00424-013-1417-7 |
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