TCF21 rs12190287 Polymorphisms Are Associated with Ventricular Septal Defects in a Chinese Population

Aims: TCF21 knockout mice display cardiac defects, including ventricular septal defects (VSDs). Functional rs12190287 polymorphisms located within the 3′ untranslated region (3′-UTR) of TCF21 were associated with a risk of coronary heart disease in the European and Eastern populations. However, whet...

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Detaylı Bibliyografya
Yayımlandı:Genet Test Mol Biomarkers
Asıl Yazarlar: Yang, Liping, Gao, Xiaobo, Luo, Haiyan, Huang, Qiuyu, Su, Dongmei, Tan, Xinyu, Lu, Cailing
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Mary Ann Liebert, Inc. 2017
Konular:
Original Articles
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC5444416/
https://ncbi.nlm.nih.gov/pubmed/28346832
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1089/gtmb.2016.0324
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