Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3 - Concepedia

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Genome-Wide Association Study to Find Modifiers for Tetralogy of Fallot in the 22q11.2 Deletion Syndrome Identifies Variants in the <i>GPR98</i> Locus on 5q14.3

DOI Full Paper Access

24

Citations

43

References

2017

Year

Tingwei Guo, Gabriela M. Repetto, Donna M. McDonald‐McGinn, Jonathan H. Chung, Hiroko Nomaru, Christopher Campbell, Anna Błońska, Anne S. Bassett, Eva W.C. Chow, Elisabeth E. Mlynarski,

Circulation Cardiovascular Genetics

Abstract

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

References

	Year	Citations

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