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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Detalles Bibliográficos
Autores principales: Tang, Wanjian, Blair, Cheavar A., Walton, Shane D., Málnási-Csizmadia, András, Campbell, Kenneth S., Yengo, Christopher M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220080/
https://www.ncbi.nlm.nih.gov/pubmed/28119616
http://dx.doi.org/10.3389/fphys.2016.00659

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5220080/
https://www.ncbi.nlm.nih.gov/pubmed/28119616
http://dx.doi.org/10.3389/fphys.2016.00659

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