Genetic Dissection of Hypertrophic Cardiomyopathy with Myocardial RNA-Seq

Hypertrophic cardiomyopathy (HCM) is an inherited disorder of the myocardium, and pathogenic mutations in the sarcomere genes myosin heavy chain 7 (MYH7) and myosin-binding protein C (MYBPC3) explain 60%–70% of observed clinical cases. The heterogeneity of phenotypes observed in HCM patients, howeve...

Descripción completa

Detalles Bibliográficos
Autores principales: Gao, Jun, Collyer, John, Wang, Maochun, Sun, Fengping, Xu, Fuyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246737/
https://www.ncbi.nlm.nih.gov/pubmed/32344918
http://dx.doi.org/10.3390/ijms21093040

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7246737/
https://www.ncbi.nlm.nih.gov/pubmed/32344918
http://dx.doi.org/10.3390/ijms21093040

Ejemplares similares