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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Detalhes bibliográficos
Publicado no:Mol Med Rep
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: D.A. Spandidos 2019
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6854592/
https://ncbi.nlm.nih.gov/pubmed/31638223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.10754
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