A Novel Mutation of the Beta Myosin Heavy Chain Gene Responsible for Familial Hypertrophic Cardiomyopathy

BACKGROUND: Hypertrophic cardiomyopathy (HCM) is the most common inherited cardiac disorder and shows high variability in genetic heterogeneity and phenotypic characteristics. The genetic etiology responsible for HCM in many individuals remains unclear. OBJECTIVE: This instigation was sought to iden...

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Veröffentlicht in:Clin Cardiol
Hauptverfasser: Wang, Juan, Xu, Shi‐Jie, Zhou, Hua, Wang, Li‐Jie, Hu, Bo, Fang, Fang, Zhang, Xu‐Min, Luo, Yi‐Wei, He, Xiao‐Yan, Zhuang, Shao‐Wei, Li, Xin‐Ming, Liu, Zhong‐Ming, Hu, Da‐Yi
Format: Artigo
Sprache:Inglês
Veröffentlicht: Wiley Periodicals, Inc. 2009
Schlagworte:
Clinical Investigations
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC6652898/
https://ncbi.nlm.nih.gov/pubmed/19645038
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/clc.20520
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