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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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Pubblicato in: | Exp Ther Med |
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Autori principali: | , , , , , , |
Natura: | Artigo |
Lingua: | Inglês |
Pubblicazione: |
D.A. Spandidos
2017
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Soggetti: | |
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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