Associated Papers
TBX20 loss-of-function mutation contributes to double outlet right ventricle.
Pan Y et al.
International Journal of Molecular Medicine, 2015
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.
Liu JJ et al.
Journal of Zhejiang University. Science. B, 2014
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