Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization (European Journal of Human Genetics, (2025), 33, 8, (989-996), 10.1038/s41431-025-01884-z)

Engel C, Rendek M, Assoumani J, Argilli E, Ariani F, Avice-Denizet AL, Bijlsma EK, Blanc P, Bruno LP, Callewaert B, Capra V, Carullo M, Chesneau B, Coppens S, Curry C, Dale B, Dahlen E, Delahaye-Duriez A, Denommé-Pichon AS, Demeer B, Dvořáková L, Fischer J, Geneviève D, Giacomini T, Handrup MM, Heron D, Hüning I, Iacomino M, Isidor B, Keren B, Kmoch S, Koolen DA, Kübler A, Laštůvková J, Le C, Levy J, Rizzo CL, Maitz S, Marlin S, Mignot C, Mirzaa G, Nagel I, Neuens S, Nosková L, Pao E, Pecková A, Plaisancie J, Porrmann J, Privitera F, Reis A, Renieri A, Rio M, Rippert A, Ryba L, Scala M, Schieving JH, Sherr EH, Shuen A, Sidlow R, Smol T, Soblet J, Striano P, Suri M, Syryn H, Tran Mau-Them F, Travessa AM, Van Gils J, Vasileiou G, Verseput JJ, Vilain C, Vincent-Delorme C, Vyhnálková E, Wakeling EL, Zacher P, Zara F, Kuentz P, Piard J (2026)

Publication Type: Journal article, Erratum

Publication year: 2026

Journal

DOI: 10.1038/s41431-026-02087-w

Abstract

Correction to: European Journal of Human Geneticshttps://doi.org/10.1038/s41431-025-01884-z, published online 25 June 2025 In the original article last name of author Emilia K. Bijlsma was incorrectly written as Bijlsmaa. The original article has been corrected.

Authors with CRIS profile

Involved external institutions

Université Marie et Louis Pasteur (prev. Université de Franche-Comté) France (FR) University of California San Francisco (UCSF) United States (USA) (US) Università degli Studi di Siena (UNISI) / University of Siena Italy (IT) Leiden University Medical Center Netherlands (NL) GCS SeqOIA France (FR) University Hospital Ghent Belgium (BE) Istituto Giannina Gaslini Italy (IT) Fondazione Policlinico Universitario Agostino Gemelli IRCCS Italy (IT) Centre Hospitalier Universitaire (CHU) de Toulouse France (FR) Hôpital Erasme Belgium (BE) Hamilton Health Sciences (HHS) Canada (CA) Hôpital Jean-Verdier France (FR) Université Bourgogne Europe France (FR) Centre Hospitalier Universitaire Amiens-Picardie (CHU Amiens-Picardie) France (FR) Motol University Hospital / Fakultní nemocnice v Motole Czech Republic (CZ) Universitätsklinikum Carl Gustav Carus Dresden Germany (DE) University of Montpellier / Université Montpellier France (FR) University of Genova / Università degli Studi di Genova Italy (IT) Aarhus University Hospital / Aarhus Universitetshospital Denmark (DK) Assistance Publique-Hôpitaux de Paris (AP-HP) France (FR) Universitätsklinikum Schleswig-Holstein (UKSH) Germany (DE) Nantes University Hospital / Centre hospitalier universitaire de Nantes (CHU) France (FR) Univerzita Karlova v Praze / Charles University in Prague Czech Republic (CZ) Radboud University Nijmegen Medical Centre / Radboudumc of voluit Radboud Universitair Medisch Centrum (UMC) Netherlands (NL) Hôpital Universitaire Robert-Debré France (FR) Valley Children's Hospital (VCH) / Children's Hospital Central California United States (USA) (US) Centre Hospitalier Régional Universitaire de Lille (CHRU de Lille) France (FR) Queen Fabiola Childrens Hospital / L'Hôpital universitaire des enfants Reine Fabiola Belgium (BE) Nottingham University Hospitals United Kingdom (GB) Great Ormond Street Hospital (GOSH) United Kingdom (GB) Kleinwachau - Sächsisches Epilepsiezentrum Radeberg gGmbH Germany (DE) Azienda ospedaliero-universitaria Senese Italy (IT) Ente Ospedaliero Cantonale Switzerland (CH) Hôpital Necker-Enfants malades France (FR) University of Washington United States (USA) (US) Center for Integrative Brain Research United States (USA) (US) IRCCS Fondazione Stella Maris Italy (IT) Université Sorbonne Paris Cité France (FR) Children's Hospital of Philadelphia United States (USA) (US) The Hospital for Sick Children (SickKids) Canada (CA) Centre Hospitalier Universitaire de Bordeaux / CHU Bordeaux France (FR)

How to cite

APA:

Engel, C., Rendek, M., Assoumani, J., Argilli, E., Ariani, F., Avice-Denizet, A.L.,... Piard, J. (2026). Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization (European Journal of Human Genetics, (2025), 33, 8, (989-996), 10.1038/s41431-025-01884-z). European Journal of Human Genetics. https://doi.org/10.1038/s41431-026-02087-w

MLA:

Engel, Camille, et al. "Correction: Comprehensive analysis of CNOT3-related neurodevelopmental disorders: phenotypic and genotypic characterization (European Journal of Human Genetics, (2025), 33, 8, (989-996), 10.1038/s41431-025-01884-z)." European Journal of Human Genetics (2026).

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