Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease
PLoS Genet
.
2021 Sep 21;17(9):e1009809.
doi: 10.1371/journal.pgen.1009809.
eCollection 2021 Sep.
Authors
Enrique Audain
,
Anna Wilsdon
,
Jeroen Breckpot
,
Jose M G Izarzugaza
,
Tomas W Fitzgerald
,
Anne-Karin Kahlert
,
Alejandro Sifrim
,
Florian Wünnemann
,
Yasset Perez-Riverol
,
Hashim Abdul-Khaliq
,
Mads Bak
,
Anne S Bassett
,
D Woodrow Benson
,
Felix Berger
,
Ingo Daehnert
,
Koenraad Devriendt
,
Sven Dittrich
,
Piers Ef Daubeney
,
Vidu Garg
,
Karl Hackmann
,
Kirstin Hoff
,
Philipp Hofmann
,
Gregor Dombrowsky
,
Thomas Pickardt
,
Ulrike Bauer
,
Bernard D Keavney
,
Sabine Klaassen
,
Hans-Heiner Kramer
,
Christian R Marshall
,
Dianna M Milewicz
,
Scott Lemaire
,
Joseph S Coselli
,
Michael E Mitchell
,
Aoy Tomita-Mitchell
,
Siddharth K Prakash
,
Karl Stamm
,
Alexandre F R Stewart
,
Candice K Silversides
,
Reiner Siebert
,
Brigitte Stiller
,
Jill A Rosenfeld
,
Inga Vater
,
Alex V Postma
,
Almuth Caliebe
,
J David Brook
,
Gregor Andelfinger
,
Matthew E Hurles
,
Bernard Thienpont
,
Lars Allan Larsen
,
Marc-Phillip Hitz
PMID:
34547032
PMCID:
PMC8454942
DOI:
10.1371/journal.pgen.1009809
Abstract
[This corrects the article DOI: 10.1371/journal.pgen.1009679.].
Publication types
Published Erratum
Grants and funding
CH/13/2/30154/BHF_/British Heart Foundation/United Kingdom
RG/15/12/31616/BHF_/British Heart Foundation/United Kingdom