Identifying novel mutations of NKX2-5 congenital heart disease patients of Chinese Minority Groups

被引:7
作者
Wang, Jing [2 ]
Chen, Qiuhong [3 ]
Wang, Lin [2 ]
Zhou, Sirui [2 ]
Cheng, Longfei [2 ]
Xie, XiaoDong [4 ]
Huang, Guoying [5 ]
Wang, Binbin [1 ,2 ]
Ma, Xu [2 ,6 ]
机构
[1] Natl Res Inst Family Planning, Ctr Genet, Beijing 100081, Peoples R China
[2] Peking Union Med Coll, Grad Sch, Beijing 100021, Peoples R China
[3] Qinghai High Altitude Med Res Inst, Xining, Peoples R China
[4] Lanzhou Univ, Sch Life Sci, Lanzhou 730000, Peoples R China
[5] Fudan Univ, Pediat Heart Ctr, Childrens Hosp, Shanghai, Peoples R China
[6] World Hlth Org Collaborating Ctr Res Human Reprod, Beijing, Peoples R China
关键词
Congenital heart disease; NKX2-5; Non-synonymous variant; Minority Groups; DNA-BINDING; PATHWAYS; DEFECTS; SYSTEM; CSX;
D O I
10.1016/j.ijcard.2010.05.041
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
[No abstract available]
引用
收藏
页码:102 / 104
页数:3
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