Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 10.1038/s41436-021-01212-y)

Skoric-Milosavljevic D, Lahrouchi N, Bosada FM, Dombrowsky G, Williams SG, Lesurf R, Tjong FVY, Walsh R, El Bouchikhi I, Breckpot J, Audain E, Ilgun A, Beekman L, Ratbi I, Strong A, Muenke M, Heide S, Muir AM, Hababa M, Cross L, Zhou D, Pastinen T, Hitz MP, Hitz MP, Abdul-Khaliq H, Berger F, Dahnert I, Dittrich S, Uebing A, Stiller B, Zackai E, Atmani S, Ouldim K, Adadi N, Steindl K, Rauch A, Brook D, Wilsdon A, Kuipers I, Blom NA, Mulder BJ, Mefford HC, Keren B, Joset P, Kruszka P, Thiffault I, Sheppard SE, Roberts A, Lodder EM, Keavney BD, Clur SAB, Mital S, Hitz MP, Christoffels VM, Postma AV, Bezzina CR (2021)

Publication Type: Journal article, Erratum

Publication year: 2021

Journal

Genetics in Medicine Nature Publishing Group: Open Access Hybrid Model Option B

DOI: 10.1038/s41436-021-01279-7

Abstract

Due to a processing error the author’s Doris Škorić-Milosavljević, Najim Lahrouchi, Alex V. Postma, Connie R. Bezzina were assigned to affiliation 38. However, affiliation 38 does not exist. In addition, the affiliations of Najim Lahrouchi, Elisabeth M. Lodder, and Connie R. Bezzina should be number 1 instead of number 2. The correct affiliation is Department of Clinical and Experimental Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands. The original article has been corrected.

Authors with CRIS profile

Sven Dittrich Professur für Kinderkardiologie

Involved external institutions

University of Amsterdam NL Netherlands (NL)

How to cite

APA:

Skoric-Milosavljevic, D., Lahrouchi, N., Bosada, F.M., Dombrowsky, G., Williams, S.G., Lesurf, R.,... Bezzina, C.R. (2021). Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 10.1038/s41436-021-01212-y). Genetics in Medicine. https://doi.org/10.1038/s41436-021-01279-7

MLA:

Skoric-Milosavljevic, Doris, et al. "Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 10.1038/s41436-021-01212-y)." Genetics in Medicine (2021).

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