Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.

Cordell HJ, Bentham J, Topf A, Zelenika D, Heath S, Mamasoula C, Cosgrove C, Blue G, Granados-Riveron J, Setchfield K, Thornborough C, Breckpot J, Soemedi R, Martin R, Rahman TJ, Hall D, van Engelen K, Moorman AF, Zwinderman AH, Barnett P, Koopmann TT, Adriaens ME, Varro A, George AL, dos Remedios C, Bishopric NH, Bezzina CR, O'Sullivan J, Gewillig M, Bu'Lock FA, Winlaw D, Bhattacharya S, Devriendt K, Brook JD, Mulder BJ, Mital S, Postma AV, Lathrop GM, Farrall M, Goodship JA, Keavney BD
Nat Genet. 2013 45 (7): 822-4

PMID: 23708191 · PMCID: PMC3793630 · DOI:10.1038/ng.2637

MeSH Terms (17)

Abnormalities, Multiple Animals Case-Control Studies Chromosomes, Human, Pair 4 Cohort Studies Female Genetic Loci Genetic Predisposition to Disease Genome-Wide Association Study Genotype Heart Defects, Congenital Heart Diseases Heart Septal Defects, Atrial Humans Male Mice Phenotype

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