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Paper Details

Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Nat Genet
102
2013
ASD, CHD, MSX1, MSX1 and STX18 genes, STX18 genes, atrial septal defect, chromosome 4p16, congenital heart disease, obstructive and cyanotic defects, susceptibility locus
Author NameAffiliation
Heather J CordellInstitute of Genetic Medicine, Newcastle University
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Release 1.2