Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy

β-myosin heavy chain (MHC) 7 (MYH7) is the dominant pathogenic gene that harbors mutations in 20–30% of cases of familial hypertrophic cardiomyopathy (HCM). The aim of this study was to elucidate the distribution and type of genetic variations among Chinese HCM families. From 2013 to 2017, the clini...

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Detalles Bibliográficos
Autores principales: Wang, Bo, Wang, Jing, Wang, Li-Feng, Yang, Fan, Xu, Lei, Li, Wen-Xia, He, Yang, Zuo, Lei, Yang, Qian-Li, Shao, Hong, Hu, Dan, Liu, Li-Wen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854592/
https://www.ncbi.nlm.nih.gov/pubmed/31638223
http://dx.doi.org/10.3892/mmr.2019.10754

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6854592/
https://www.ncbi.nlm.nih.gov/pubmed/31638223
http://dx.doi.org/10.3892/mmr.2019.10754

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