Published erratum: Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein

Authors

Elke de Boer, Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
Charlotte W. Ockeloen, Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands.
Rosalie A. Kampen, Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Juliet E. Hampstead, Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands; Radboud Institute for Molecular Life Sciences, Radboudumc, Nijmegen, The Netherlands.
Alexander J. Dingemans, Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
Dmitrijs Rots, Department of Human Genetics, Radboudumc, Nijmegen, The Netherlands; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
Lukas Lütje, Language and Genetics Department, Max Planck Institute for Psycholinguistics, Nijmegen, The Netherlands.
Tazeen Ashraf, Department of Clinical Genetics, Great Ormond Street Hospital for Children NHS Foundation Trust, London, United Kingdom; Clinical Genetics, Guy's and St Thomas' NHS Foundation Trust, London, United Kingdom.
Rachel Baker, Advocate Aurora HealthFollow
Mouna Barat-Houari, Genetic Laboratory of Rare and Autoinflammatory Diseases, Department of Medical Genetics, Rare Diseases and Personalized Medicine, Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
Brad Angle, Advocate Aurora HealthFollow
et al

Recommended Citation

de Boer E, Ockeloen CW, Kampen RA, et al. Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. Genet Med. 2023;25(11):100962. doi:10.1016/j.gim.2023.100962

Affiliations

Advocate Children's Hospital, Park Ridge, IL

Abstract

Erratum for

• Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein. de Boer E, Ockeloen CW, Kampen RA, et al. Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein [published correction appears in Genet Med. 2023;100962]. Genet Med. 2022 Oct;24(10):2051-2064. doi: 10.1016/j.gim.2022.06.007

Type

Article

PubMed ID

37658852