Rare variants in NR2F2 cause congenital heart defects in humans

Rare variants in NR2F2 cause congenital heart defects in humans

Congenital heart defects (CHDs) are the most common birth defect worldwide and are a leading cause of neonatal mortality. Nonsyndromic atrioventricular septal defects (AVSDs) are an important subtype of CHDs for which the genetic architecture is poorly understood. We performed exome sequencing in 13...

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Main Authors: Al Turki, Saeed (Author), Manickaraj, Ashok K. (Author), Mercer, Catherine L. (Author), Gerety, Sebastian S. (Author), Hitz, Marc-Phillip (Author), Lindsay, Sarah (Author), D'Alessandro, Lisa C.A (Author), Swaminathan, G. Jawahar (Author), Bentham, Jamie (Author), Arndt, Anne-Karin (Author), Low, Jacoba (Author), Breckpot, Jeroen (Author), Gewillig, Marc (Author), Thienpont, Bernard (Author), Abdul-Khaliq, Hashim (Author), Harnack, Christine (Author), Hoff, Kirstin (Author), Kramer, Hans-Heiner (Author), Schubert, Stephan (Author), Siebert, Reiner (Author), Toka, Okan (Author), Cosgrove, Catherine (Author), Watkins, Hugh (Author), Lucassen, Anneke M. (Author), O'Kelly, Ita M. (Author), Salmon, Anthony P. (Author), Bu'Lock, Frances A. (Author), Granados-Riveron, Javier (Author), Setchfield, Kerry (Author), Thornborough, Chris (Author), Brook, J. David (Author), Mulder, Barbara (Author), Klaassen, Sabine (Author), Bhattacharya, Shoumo (Author), Devriendt, Koen (Author), FitzPatrick, David F. (Author), Wilson, David I. (Author), Mital, Seema (Author), Hurles, Matthew E. (Author)
Format: Article
Language:English
Published: 2014-04-03.
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