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In their interesting manuscript, Tomita-Mitchell et al present four novel GATA4 sequence variations as pathogenic substrates for congenital heart disease (CHD) in humans.1 CHD is the most common birth defect and affects almost 1% of all newborns. With the substantial improvement in surgical approaches that has occurred over the past decades, the number of adults living with CHD has increased. This fact demands better insights into the genetics and heredity of CHD.
The authors identified a variety of synonymous variants with a potential effect on the translational kinetics of GATA4. Interestingly, all 18 CHD-associated synonymous sequence variants were exclusively found in patients with septal or conotruncal …
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