Screening of MYH7 gene mutation sites in hypertrophic cardiomyopathy and its significance

BACKGROUND: There have been few reports of mutations in the beta-myosin heavy chain (MYH7) gene in hypertrophic cardiomyopathy (HCM), which is associated with sudden cardiac death caused by HCM. This study aimed to screen the mutation sites in the sarcomeric gene MYH7 in Chinese patients with HCM. W...

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Detalhes bibliográficos
Publicado no:Chin Med J (Engl)
Main Authors: Liu, Hui-Ting, Ji, Fang-Fang, Wei, Ling, Zuo, An-Jun, Gao, Yu-Xiu, Qi, Lin, Jin, Bu, Wang, Ji-Gang, Zhao, Peng
Formato: Artigo
Idioma:Inglês
Publicado em: Wolters Kluwer Health 2019
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Original Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC6940073/
https://ncbi.nlm.nih.gov/pubmed/31856055
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/CM9.0000000000000428
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