Correction: Dominant negative ADA2 mutations cause ADA2 deficiency in heterozygous carriers
Marjon Wouters, Lisa Ehlers, Wout Van Eynde, Meltem Ece Kars, Selket Delafontaine, Verena Kienapfel, Mariia Dzhus, Rik Schrijvers, Petra De Haes, Sofie Struyf, Giorgia Bucciol, Yuval Itan, Alexandre Bolze, Arnout Voet, Anneleen Hombrouck, Leen Moens, Benson Ogunjimi
Abstract
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsAmino Acid Enzymes and Metabolism · Biotin and Related Studies · Genomics and Rare Diseases
Vol. 222, No. 11 | https://doi.org/10.1084/jem.20250499 | August 27, 2025
The authors regret that there were errors in the originally published Fig. 8 and the related Table S9. In Fig. 8, a mistake during data analysis skewed the forest plots uniformly. In Table S9, the UK Biobank GeneBass odds ratio data and the UK Biobank AZPhewas odds ratio and P value data were incorrect. These errors do not affect the conclusions of the study, and there are no changes to the main text or figure legends. The original and corrected Fig. 8 are shown here, and Table S9 has been replaced online. The errors appear in print and in files downloaded before December 29, 2025.