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Modulating Beta-Cardiac Myosin Function at the Molecular and Tissue Levels

Inherited cardiomyopathies are a common form of heart disease that are caused by mutations in sarcomeric proteins with beta cardiac myosin (MYH7) being one of the most frequently affected genes. Since the discovery of the first cardiomyopathy associated mutation in beta-cardiac myosin, a major goal...

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Detalhes bibliográficos
Publicado no:Front Physiol
Main Authors: Tang, Wanjian, Blair, Cheavar A., Walton, Shane D., Málnási-Csizmadia, András, Campbell, Kenneth S., Yengo, Christopher M.
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5220080/
https://ncbi.nlm.nih.gov/pubmed/28119616
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphys.2016.00659
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