Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation

Mutations in TNNC1—the gene encoding cardiac troponin C (cTnC)—that have been associated with hypertrophic cardiomyopathy (HCM) and cardiac dysfunction may also affect Ca(2+)-regulation and function of slow skeletal muscle since the same gene is expressed in both cardiac and slow skeletal muscle. Th...

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Detalles Bibliográficos
Autores principales: Veltri, Tiago, Landim-Vieira, Maicon, Parvatiyar, Michelle S., Gonzalez-Martinez, David, Dieseldorff Jones, Karissa M., Michell, Clara A., Dweck, David, Landstrom, Andrew P., Chase, P. Bryant, Pinto, Jose R.
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/PMC5397416/
https://www.ncbi.nlm.nih.gov/pubmed/28473771
http://dx.doi.org/10.3389/fphys.2017.00221

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5397416/
https://www.ncbi.nlm.nih.gov/pubmed/28473771
http://dx.doi.org/10.3389/fphys.2017.00221

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