Hypertrophic Cardiomyopathy: From Phenotype and Pathogenesis to Treatment

Hypertrophic cardiomyopathy (HCM) is a very common inherited cardiovascular disease (CAD) and the incidence is about 1/500 of the common population. It is caused by more than 1,400 mutations in 11 or more genes encoding the proteins of the cardiac sarcomere. HCM presents a heterogeneous clinical pro...

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Detalles Bibliográficos
Autores principales: Cheng, Zeyi, Fang, Tingting, Huang, Jinglei, Guo, Yingqiang, Alam, Mahboob, Qian, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Cardiovascular Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572854/
https://www.ncbi.nlm.nih.gov/pubmed/34760939
http://dx.doi.org/10.3389/fcvm.2021.722340

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8572854/
https://www.ncbi.nlm.nih.gov/pubmed/34760939
http://dx.doi.org/10.3389/fcvm.2021.722340

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