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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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Detaylı Bibliyografya
Yayımlandı:Clin Cardiol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Wiley Periodicals, Inc. 2009
Konular:
Online Erişim: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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