Abstract
马玉龙,李晓梅,杨毅宁,马依彤,谢翔,李海霞,刘芬.Tbx20基因多态性与新疆维吾尔族人群先天性房间隔缺损的相关性研究[J].Chinese journal of Epidemiology,2014,35(7):872-873
Tbx20基因多态性与新疆维吾尔族人群先天性房间隔缺损的相关性研究
Association between the SNPs of human Tbx20 gene and congenital atrial septal defects in Uygur population of Xinjiang region
Received:December 01, 2013  
DOI:10.3760/cma.j.issn.0254-6450.2014.07.026
KeyWord: 先天性心脏病  T-box 转录因子  单核苷酸多态性
English Key Word: Congenital heart disease  T-box transcription factor  Single nucleotide polymorphism
FundProject:新疆维吾尔自治区自然科学基金(2012211A062)
Author NameAffiliationE-mail
Ma Yulong Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
Li Xiaomei Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China lixm505@163.com 
Yang Yining Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
Ma Yitong Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
Xie Xiang Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
Li Haixia Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
Liu Fen Department of Cardiology, the First Affiliated Hospital to Xinjiang Medical University, Urumqi 830054, China  
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Abstract:
      研究显示, Tbx20 基因在心脏发育过程中具有重要作用, Tbx20 敲除的成年鼠表现出轻度房间隔畸形[1]。Kirk 等[2]在房间隔缺损家系中发现Tbx20 基因存在2 个突变。
English Abstract:
      
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