Genetic analysis of monoallelic double MYH7 mutations responsible for familial hypertrophic cardiomyopathy

β-myosin heavy chain (MHC) 7 (MYH7) is the dominant pathogenic gene that harbors mutations in 20–30% of cases of familial hypertrophic cardiomyopathy (HCM). The aim of this study was to elucidate the distribution and type of genetic variations among Chinese HCM families. From 2013 to 2017, the clini...

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Detaylı Bibliyografya
Yayımlandı:Mol Med Rep
Asıl Yazarlar: Wang, Bo, Wang, Jing, Wang, Li-Feng, Yang, Fan, Xu, Lei, Li, Wen-Xia, He, Yang, Zuo, Lei, Yang, Qian-Li, Shao, Hong, Hu, Dan, Liu, Li-Wen
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: D.A. Spandidos 2019
Konular:
Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC6854592/
https://ncbi.nlm.nih.gov/pubmed/31638223
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.10754
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