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A novel variant in TBX20 (p.D176N) identified by whole-exome sequencing in combination with a congenital heart disease related gene filter is associated with familial atrial septal defect 期刊论文
Journal of Zhejiang University. Science B, Biomedicine & Biotechnology, 2014, 卷号: 15, 期号: 9, 页码: 830-837
作者:  Liu Jijia;  Fan Liangliang;  Chen Jinlan;  Tan Zhiping;  Yang Yifeng
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