Inherited Cardiomyopathies and the Role of Mutations in Non-coding Regions of the Genome

Cardiomyopathies (CMs) are a group of cardiac pathologies caused by an intrinsic defect within the myocardium. The relative contribution of genetic mutations in the pathogenesis of certain CMs, such as hypertrophic cardiomyopathy (HCM), arrythmogenic right/left ventricular cardiomyopathy (ARVC) and...

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Detalles Bibliográficos
Autores principales: Salman, Oday F., El-Rayess, Hebah M., Abi Khalil, Charbel, Nemer, Georges, Refaat, Marwan M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028572/
https://www.ncbi.nlm.nih.gov/pubmed/29998127
http://dx.doi.org/10.3389/fcvm.2018.00077

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6028572/
https://www.ncbi.nlm.nih.gov/pubmed/29998127
http://dx.doi.org/10.3389/fcvm.2018.00077

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