Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study

Affiliations

• ¹ Département de Génétique, Hôpital Robert-Debré, Paris, France. alix.paulet@hotmail.fr.
• ² Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.
• ³ Département de Génétique, Hôpital Robert-Debré, Paris, France.
• ⁴ Laboratoire Cerba, Saint-Ouen l'Aumône, France.
• ⁵ UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland.
• ⁶ Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK.
• ⁷ Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK.
• ⁸ Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland.
• ⁹ Oulu University Hospital and University of Oulu, Oulu, Finland.
• ¹⁰ Centre de Génétique Humaine, CHU Besançon, Besançon, France.
• ¹¹ Service de Génétique Médicale, CHU de Montpellier, Montpellier, France.
• ¹² South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK.
• ¹³ Clinical Genetics, Children's Health Ireland, Dublin, Ireland.
• ¹⁴ Department of Neuropediatrics, University Children's Hospital, Tuebingen, Germany.
• ¹⁵ Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France.
• ¹⁶ University Hospitals of Geneva, Geneva, Switzerland.
• ¹⁷ Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
• ¹⁸ Human Genetik, Syddansk Universitet, Odense, Denmark.
• ¹⁹ Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland.
• ²⁰ Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
• ²¹ Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
• ²² Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
• ²³ Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.
• ²⁴ Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France.
• ²⁵ Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France.
• ²⁶ UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.
• ²⁷ Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia.
• ²⁸ Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
• ²⁹ UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
• ³⁰ Génétique Médicale, CHU de Caen, Caen, France.
• ³¹ Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
• ³² MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK.
• ³³ H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
• ³⁴ Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
• ³⁵ Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.
• ³⁶ Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA.
• ³⁷ Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland.
• ³⁸ Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.
• ³⁹ University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France.
• ⁴⁰ Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France.
• ⁴¹ Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
• ⁴² UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France.
• ⁴³ Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs », Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France.
• ⁴⁴ Pediatric Neurology and Muscular Diseases Unit, IRCCS Istituto Giannina Gaslini, Genoa, Italy.
• ⁴⁵ Department of Neurosciences, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.
• ⁴⁶ Division of Child Neuropsychiatry, Martini Hospital, Torino, Italy.
• ⁴⁷ Laboratorio Di Genetica Medica, Bergamo, Italy.
• ⁴⁸ Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands.