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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Enregistré dans:
Détails bibliographiques
Publié dans:Clin Cardiol
Auteurs principaux: 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
Langue:Inglês
Publié: Wiley Periodicals, Inc. 2009
Sujets:
Clinical Investigations
Accès en ligne: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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