Correction: A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells

Affiliations

¹ Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
² Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
³ Department of Pediatrics, Hospital del Santa Creu y Sant Pau, Barcelona, Spain.
⁴ Department of Pediatric Neurology, Hospital Virgen de la Arrixaca, Murcia, Madrid, Spain.
⁵ Department of Pediatric Neurology, Hospital de Manises, Valencia, Spain.
⁶ Department of Genetics, Consorcio Hospital General de Valencia, Valencia, Spain.
⁷ Department of Pediatrics, Hospital de Requena, Valencia, Spain.
⁸ Genetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.
⁹ Movement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII and European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain.
¹⁰ Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands. david.koolen@radboudumc.nl.
¹¹ Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.
¹² Division of Clinical and Metabolic Genetics, Department of Pediatrics, the Hospital for Sick Children, University of Toronto, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.

Published Erratum

Zain Awamleh et al. Eur J Hum Genet. 2024 Mar.

. 2024 Mar;32(3):366.

doi: 10.1038/s41431-024-01561-7.

¹ Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada.
² Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands.
³ Department of Pediatrics, Hospital del Santa Creu y Sant Pau, Barcelona, Spain.
⁴ Department of Pediatric Neurology, Hospital Virgen de la Arrixaca, Murcia, Madrid, Spain.
⁵ Department of Pediatric Neurology, Hospital de Manises, Valencia, Spain.
⁶ Department of Genetics, Consorcio Hospital General de Valencia, Valencia, Spain.
⁷ Department of Pediatrics, Hospital de Requena, Valencia, Spain.
⁸ Genetics Unit, Universitat Pompeu Fabra, Hospital del Mar Research Institute (IMIM) and CIBERER, Barcelona, Spain.
⁹ Movement Disorders Unit, Institut de Recerca Sant Joan de Déu, CIBERER-ISCIII and European Reference Network for Rare Neurological Diseases (ERN-RND), Barcelona, Spain.
¹⁰ Department of Human Genetics, Radboud University Medical Center, Donders Institute for Brain, Cognition, and Behavior, Nijmegen, The Netherlands. david.koolen@radboudumc.nl.
¹¹ Genetics and Genome Biology Program, Research Institute, the Hospital for Sick Children, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.
¹² Division of Clinical and Metabolic Genetics, Department of Pediatrics, the Hospital for Sick Children, University of Toronto, Toronto, ON, M5G 1×8, Canada. rweksb@sickkids.ca.

No abstract available

Erratum for

A new blood DNA methylation signature for Koolen-de Vries syndrome: Classification of missense KANSL1 variants and comparison to fibroblast cells.
Awamleh Z, Choufani S, Wu W, Rots D, Dingemans AJM, Nadif Kasri N, Boronat S, Ibañez-Mico S, Cuesta Herraiz L, Ferrer I, Martínez Carrascal A, Pérez-Jurado LA, Aznar Lain G, Ortigoza-Escobar JD, de Vries BBA, Koolen DA, Weksberg R. Awamleh Z, et al. Eur J Hum Genet. 2024 Mar;32(3):324-332. doi: 10.1038/s41431-024-01538-6. Epub 2024 Jan 29. Eur J Hum Genet. 2024. PMID: 38282074 Free PMC article.