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
From embryogenesis to adulthood: Critical role for GATA factors in heart development and function.
Whitcomb J et al.
Iubmb Life, 2020
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.
Kassab K et al.
Molecular Genetics & Genomic Medicine, 2016
An excess of deleterious variants in VEGF-A pathway genes in Down-syndrome-associated atrioventricular septal defects.
Ackerman C et al.
American Journal of Human Genetics, 2012
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