Familial hypertrophic cardiomyopathy: functional variance among individual cardiomyocytes as a trigger of FHC-phenotype development

Familial hypertrophic cardiomyopathy (FHC) is the most frequent inherited cardiac disease. It has been related to numerous mutations in many sarcomeric and even some non-sarcomeric proteins. So far, however, no common mechanism has been identified by which the many different mutations in different s...

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Detalles Bibliográficos
Autores principales: Brenner, Bernhard, Seebohm, Benjamin, Tripathi, Snigdha, Montag, Judith, Kraft, Theresia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Physiology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193225/
https://www.ncbi.nlm.nih.gov/pubmed/25346696
http://dx.doi.org/10.3389/fphys.2014.00392

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4193225/
https://www.ncbi.nlm.nih.gov/pubmed/25346696
http://dx.doi.org/10.3389/fphys.2014.00392

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