Associated Papers
Whole-Exome Sequencing Identifies Novel GATA5/6 Variants in Right-Sided Congenital Heart Defects.
Zodanu GKE et al.
International Journal of Molecular Sciences, 2025
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
GATA5 mutation homozygosity linked to a double outlet right ventricle phenotype in a Lebanese patient.
Kassab K et al.
Molecular Genetics & Genomic Medicine, 2016
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