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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Detalhes bibliográficos
Publicado no:Clin Cardiol
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Wiley Periodicals, Inc. 2009
Assuntos:
Clinical Investigations
Acesso em linha: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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