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Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease.
Audain, Enrique; Wilsdon, Anna; Breckpot, Jeroen; Izarzugaza, Jose M G; Fitzgerald, Tomas W; Kahlert, Anne-Karin; Sifrim, Alejandro; Wünnemann, Florian; Perez-Riverol, Yasset; Abdul-Khaliq, Hashim; Bak, Mads; Bassett, Anne S; Benson, D Woodrow; Berger, Felix; Daehnert, Ingo; Devriendt, Koenraad; Dittrich, Sven; Daubeney, Piers Ef; Garg, Vidu; Hackmann, Karl; Hoff, Kirstin; Hofmann, Philipp; Dombrowsky, Gregor; Pickardt, Thomas; Bauer, Ulrike; Keavney, Bernard D; Klaassen, Sabine; Kramer, Hans-Heiner; Marshall, Christian R; Milewicz, Dianna M; Lemaire, Scott; Coselli, Joseph S; Mitchell, Michael E; Tomita-Mitchell, Aoy; Prakash, Siddharth K; Stamm, Karl; Stewart, Alexandre F R; Silversides, Candice K; Siebert, Reiner; Stiller, Brigitte; Rosenfeld, Jill A; Vater, Inga; Postma, Alex V; Caliebe, Almuth; Brook, J David; Andelfinger, Gregor; Hurles, Matthew E; Thienpont, Bernard; Larsen, Lars Allan; Hitz, Marc-Phillip.
PLoS Genet ; 17(9): e1009809, 2021 Sep.
Article in En | MEDLINE | ID: mdl-34547032
ABSTRACT
[This corrects the article DOI 10.1371/journal.pgen.1009679.].
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2021 Document type: Article
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Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Language: En Journal: PLoS Genet Journal subject: GENETICA Year: 2021 Document type: Article