Whole-exome sequencing reveals MYH7 p.R671C mutation in three different phenotypes of familial hypertrophic cardiomyopathy

Familial hypertrophic cardiomyopathy (HCM) is one of the most common types of genetic heart disorder and features high genetic heterogeneity. HCM is a major cause of sudden cardiac death and also an important cause of heart failure-related disability. A pedigree with suspected familial HCM was recru...

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Detalles Bibliográficos
Autores principales: Yu, Wei, Huang, Mi-Mi, Zhang, Guo-Hong, Wang, Wei, Chen, Chun-Juan, Cheng, Ji-Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311224/
https://www.ncbi.nlm.nih.gov/pubmed/34345284
http://dx.doi.org/10.3892/etm.2021.10434

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8311224/
https://www.ncbi.nlm.nih.gov/pubmed/34345284
http://dx.doi.org/10.3892/etm.2021.10434

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