Correction: Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. PLoS Genet 2021 Sep;17(9):e1009809
Date
09/22/2021Pubmed ID
34547032Pubmed Central ID
PMC8454942DOI
10.1371/journal.pgen.1009809Scopus ID
2-s2.0-85116272362 (requires institutional sign-in at Scopus site)Abstract
[This corrects the article DOI: 10.1371/journal.pgen.1009679.].
Author List
Audain E, Wilsdon A, Breckpot J, Izarzugaza JMG, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson DW, Berger F, Daehnert I, Devriendt K, Dittrich S, Daubeney PE, Garg V, Hackmann K, Hoff K, Hofmann P, Dombrowsky G, Pickardt T, Bauer U, Keavney BD, Klaassen S, Kramer HH, Marshall CR, Milewicz DM, Lemaire S, Coselli JS, Mitchell ME, Tomita-Mitchell A, Prakash SK, Stamm K, Stewart AFR, Silversides CK, Siebert R, Stiller B, Rosenfeld JA, Vater I, Postma AV, Caliebe A, Brook JD, Andelfinger G, Hurles ME, Thienpont B, Larsen LA, Hitz MPAuthors
Michael Edward Mitchell MD Chief, Professor in the Surgery department at Medical College of WisconsinAoy Tomita Mitchell PhD Professor in the Surgery department at Medical College of Wisconsin