Correction to: European Journal of Human Genetics https://doi.org/10.1038/s41431-024-01560-8, published online 15 February 2024
In the original version of this article, the given and family names of Samuel Groeschel were incorrectly structured. The name was displayed correctly in all versions at the time of publication.
The authors, Adam Ostendorf, Christiane Zweier, Thomas Smol, Marjolaine Willems, Laurence Faivre, Marcello Scala, Pasquale Striano, Irene Bagnasco, Daniel Koboldt, Maria Iascone, Manon Suerink were missing from the author list. Moreover, the author contribution texts have been updated in accordance with addition of authors.
The original article has been corrected.
Author information
Authors and Affiliations
Département de Génétique, Hôpital Robert-Debré, Paris, France
Alix Paulet, Faustine Ageorges, Jonathan Levy, Alain Verloes & Lyse Ruaud
Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK
Cavan Bennett-Ness & Catherine M Abbott
Laboratoire Cerba, Saint-Ouen l’Aumône, France
Detlef Trost
UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland
Andrew Green
Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK
David Goudie
Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK
Rosalyn Jewell
Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland
Minna Kraatari-Tiri
Oulu University Hospital and University of Oulu, Oulu, Finland
Minna Kraatari-Tiri
Centre de Génétique Humaine, CHU Besançon, Besançon, France
Juliette PIARD
Service de Génétique Médicale, CHU de Montpellier, Montpellier, France
Christine Coubes
South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK
Wayne Lam
Clinical Genetics, Children’s Health Ireland, Dublin, Ireland
Sally Ann Lynch
Department of Neuropediatrics, University Children’s Hospital, Tuebingen, Germany
Samuel Groeschel
Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France
Francis Ramond
University Hospitals of Geneva, Geneva, Switzerland
Joël Fluss
Department of Clinical Genetics, Odense University Hospital, Odense, Denmark
Christina Fagerberg
Human Genetik, Syddansk Universitet, Odense, Denmark
Charlotte Brasch Andersen
Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland
Konstantinos Varvagiannis
Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands
Tjitske Kleefstra & Elke de Boer
Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands
Tjitske Kleefstra & Elke de Boer
Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands
Tjitske Kleefstra & Elke de Boer
Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands
Tjitske Kleefstra
Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France
Bénédicte Gérard
Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France
Mélanie Fradin
UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France
Antonio Vitobello
Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia
Romano Tenconi
Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France
Anne-Sophie Denommé-Pichon
UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France
Anne-Sophie Denommé-Pichon
Génétique Médicale, CHU de Caen, Caen, France
Aline Vincent-Devulder
Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany
Tobias Haack, Mona Grimmel & Angelika Riess
MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK
Joseph A Marsh
H C Andersen Children’s Hospital, Odense University Hospital, Odense, Denmark
Lone Walentin Laulund
Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children’s Hospital, Phoenix, AZ, USA
Sergio Padilla-Lopez, Somayeh Bakhtiari & Michael C Kruer
Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children’s Hospital, Colombus, OH, USA
Adam Ostendorf, Daniel Koboldt & Daniel Koboldt
Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA
Adam Ostendorf
Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland
Christiane Zweier
Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany
Christiane Zweier
University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France
Thomas Smol
Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France
Marjolaine Willems
Centre Hospitalier Universitaire de Montpellier, Montpellier, France
Marjolaine Willems
UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France
Laurence Faivre
Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France
Laurence Faivre
Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy
Marcello Scala & Pasquale Striano
Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy
Marcello Scala & Pasquale Striano
Division of Child Neuropsychiatry, Martini Hospital, Torino, Italy
Irene Bagnasco
Laboratorio Di Genetica Medica, Bergamo, Italy
Maria Iascone
Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands
Manon Suerink
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Correspondence to Alix Paulet.
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Paulet, A., Bennett-Ness, C., Ageorges, F. et al. Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study. Eur J Hum Genet (2024). https://doi.org/10.1038/s41431-024-01606-x
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DOI: https://doi.org/10.1038/s41431-024-01606-x
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