Ontology highlight
ABSTRACT:
SUBMITTER: Xu J
PROVIDER: S-EPMC3940663 | biostudies-literature | 2014
REPOSITORIES: biostudies-literature
Xu Jing J Lin Yuan Y Si Linjie L Jin Guangfu G Dai Juncheng J Wang Cheng C Chen Jiaping J Da Min M Hu Yuanli Y Yi Chenlong C Hu Zhibin Z Shen Hongbing H Mo Xuming X Chen Yijiang Y Wang Xiaowei X
PloS one 20140303 3
A recent genome-wide association study (GWAS) has identified a new subset of susceptibility loci of Tetralogy of Fallot (TOF), one form of cyanotic congenital heart disease (CHD), on chromosomes 10p11, 10p14, 12q24, 13q31, 15q13 and 16q12 in Europeans. In the current study, we conducted a case-control study in a Chinese population including 1,010 CHD cases [atrial septal defect (ASD), ventricular septal defect (VSD) and TOF] and 1,962 controls to evaluate the associations of these loci with risk ...[more]