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

✍ Scribed by Cordell, Heather J; Bentham, Jamie; Topf, Ana; Zelenika, Diana; Heath, Simon; Mamasoula, Chrysovalanto; Cosgrove, Catherine; Blue, Gillian; Granados-Riveron, Javier; Setchfield, Kerry; Thornborough, Chris; Breckpot, Jeroen; Soemedi, Rachel; Martin, Ruairidh; Rahman, Thahira J; Hall, Darroch; van Engelen, Klaartje; Moorman, Antoon F M; Zwinderman, Aelko H; Barnett, Phil; Koopmann, Tamara T; Adriaens, Michiel E; Varro, Andras; George, Alfred L; dos Remedios, Christobal; Bishopric, Nanette H; Bezzina, Connie R; O'Sullivan, John; Gewillig, Marc; Bu'Lock, Frances A; Winlaw, David; Bhattacharya, Shoumo; Devriendt, Koen; Brook, J David; Mulder, Barbara J M; Mital, Seema; Postma, Alex V; Lathrop, G Mark; Farrall, Martin; Goodship, Judith A; Keavney, Bernard D

• Book ID: 120585429
• Publisher: Nature Publishing Group
• Year: 2013
• Tongue: English
• Weight: 333 KB
• Volume: 45
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng.2637