Rare Variants in NR2F2 Cause Congenital Heart Defects in Humans
Am J Hum Genet
.
2016 Mar 3;98(3):592.
doi: 10.1016/j.ajhg.2016.02.016.
Epub 2016 Mar 3.
Authors
Saeed Al Turki
,
Ashok K Manickaraj
,
Catherine L Mercer
,
Sebastian S Gerety
,
Marc-Phillip Hitz
,
Sarah Lindsay
,
Lisa C A D'Alessandro
,
G Jawahar Swaminathan
,
Jamie Bentham
,
Anne-Karin Arndt
,
Jacoba Louw
,
Jeroen Breckpot
,
Marc Gewillig
,
Bernard Thienpont
,
Hashim Abdul-Khaliq
,
Christine Harnack
,
Kirstin Hoff
,
Hans-Heiner Kramer
,
Stephan Schubert
,
Reiner Siebert
,
Okan Toka
,
Catherine Cosgrove
,
Hugh Watkins
,
Anneke M Lucassen
,
Ita M O'Kelly
,
Anthony P Salmon
,
Frances A Bu'Lock
,
Javier Granados-Riveron
,
Kerry Setchfield
,
Chris Thornborough
,
J David Brook
,
Barbara Mulder
,
Sabine Klaassen
,
Shoumo Bhattacharya
,
Koen Devriendt
,
David R FitzPatrick
;
UK10K Consortium
;
David I Wilson
,
Seema Mital
,
Matthew E Hurles
PMID:
28863274
PMCID:
PMC4800046
DOI:
10.1016/j.ajhg.2016.02.016
No abstract available
Publication types
Published Erratum
Grants and funding
RG/10/17/28553/BHF_/British Heart Foundation/United Kingdom
RG/13/10/30376/BHF_/British Heart Foundation/United Kingdom