Skip to main navigation Skip to search Skip to main content

Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)

  • German Competence Network for Congenital Heart Defects
  • Amsterdam UMC - University of Amsterdam
  • Kiel University
  • University of Manchester
  • University of Toronto
  • Sidi Mohamed Ben Abdellah University
  • KU Leuven
  • Mohammed V University in Rabat
  • Ministry of Health, Morocco
  • The Children's Hospital of Philadelphia
  • National Institutes of Health
  • Sorbonne Université
  • University of Washington
  • Children's Mercy Hospitals and Clinics
  • University of Missouri at Kansas City
  • Saarland University
  • Deutsches Herzzentrum Berlin
  • Fresenius AG
  • Friedrich-Alexander University Erlangen-Nürnberg
  • University of Freiburg
  • University of Zurich
  • University of Nottingham
  • Leiden University
  • Harvard University
  • Manchester University NHS Foundation Trust
  • German Centre for Cardiovascular Research
  • Wellcome Trust Sanger Centre

Research output: Contribution to journalComment/debate

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.

Original languageEnglish
Pages (from-to)2013
Number of pages1
JournalGenetics in Medicine
Volume23
Issue number10
DOIs
Publication statusPublished - Oct 2021
Externally publishedYes

Fingerprint

Dive into the research topics of 'Correction to: Rare variants in KDR, encoding VEGF Receptor 2, are associated with tetralogy of Fallot (Genetics in Medicine, (2021), 23, 10, (1952-1960), 10.1038/s41436-021-01212-y)'. Together they form a unique fingerprint.

Cite this