Associated Papers
Identification of a novel GATA binding protein 5 variant (c.830C>T/p.P277L) damaging the nuclear translocation and causing tetralogy of Fallot.
Jin JY et al.
Qjm : Monthly Journal of the Association of Physicians, 2022
Genetic insights into non-syndromic Tetralogy of Fallot.
Althali NJ et al.
Frontiers in Physiology, 2022
Multiple gene variations contributed to congenital heart disease via GATA family transcriptional regulation.
Qian Y et al.
Journal of Translational Medicine, 2017
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