Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the GPR98 Locus on 5q14.3 [Original Articles]

Conclusions—
In conclusion, common variants may contribute to TOF in 22q11.2DS and may function in cardiac outflow tract development.

Source: Circulation: Cardiovascular Genetics - October 12, 2017 Category: Cardiology Authors: Guo, T., Repetto, G. M., McDonald McGinn, D. M., Chung, J. H., Nomaru, H., Campbell, C. L., Blonska, A., Bassett, A. S., Chow, E. W. C., Mlynarski, E. E., Swillen, A., Vermeesch, J., Devriendt, K., Gothelf, D., Carmel, M., Michaelovsky, E., Schneider, M., Tags: Translational Studies, Genetic, Association Studies, Congenital Heart Disease Original Articles Source Type: research