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
Somatic GATA5 mutations in sporadic tetralogy of Fallot.
Huang RT et al.
International Journal of Molecular Medicine, 2014
Prevalence and spectrum of GATA5 mutations associated with congenital heart disease.
Jiang JQ et al.
International Journal of Cardiology, 2013
Mutational spectrum of the GATA5 gene associated with familial atrial fibrillation.
Yang YQ et al.
International Journal of Cardiology, 2012
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