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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Detalles Bibliográficos
Autores principales: Liu, Hui-Ting, Ji, Fang-Fang, Wei, Ling, Zuo, An-Jun, Gao, Yu-Xiu, Qi, Lin, Jin, Bu, Wang, Ji-Gang, Zhao, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2019
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940073/
https://www.ncbi.nlm.nih.gov/pubmed/31856055
http://dx.doi.org/10.1097/CM9.0000000000000428

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6940073/
https://www.ncbi.nlm.nih.gov/pubmed/31856055
http://dx.doi.org/10.1097/CM9.0000000000000428

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