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Echocardiographic characterization of hypertrophic cardiomyopathy in Chinese patients with myosin-binding protein C3 mutations

Hypertrophic cardiomyopathy (HCM) is a common autosomal dominant cardiac disease, affecting 1 in 500 people. Myosin-binding protein C3 (MyBPC3) gene mutations are the most common genetic cause of HCM. However, the prevalence of the MyBPC3 gene mutation in Chinese patients with HCM, and their echocar...

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Dettagli Bibliografici
Pubblicato in:Exp Ther Med
Autori principali: Zhao, Bei, Wang, Shouli, Chen, Jinsong, Ji, Yali, Wang, Jing, Tian, Xiaoli, Zhi, Guang
Natura: Artigo
Lingua:Inglês
Pubblicazione: D.A. Spandidos 2017
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5403175/
https://ncbi.nlm.nih.gov/pubmed/28450932
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/etm.2017.4089
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