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Correction: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study.
Paulet, Alix; Bennett-Ness, Cavan; Ageorges, Faustine; Trost, Detlef; Green, Andrew; Goudie, David; Jewell, Rosalyn; Kraatari-Tiri, Minna; Piard, Juliette; Coubes, Christine; Lam, Wayne; Lynch, Sally Ann; Groeschel, Samuel; Ramond, Francis; Fluss, Joël; Fagerberg, Christina; Brasch Andersen, Charlotte; Varvagiannis, Konstantinos; Kleefstra, Tjitske; Gérard, Bénédicte; Fradin, Mélanie; Vitobello, Antonio; Tenconi, Romano; Denommé-Pichon, Anne-Sophie; Vincent-Devulder, Aline; Haack, Tobias; Marsh, Joseph A; Laulund, Lone Walentin; Grimmel, Mona; Riess, Angelika; de Boer, Elke; Padilla-Lopez, Sergio; Bakhtiari, Somayeh; Ostendorf, Adam; Zweier, Christiane; Smol, Thomas; Willems, Marjolaine; Faivre, Laurence; Scala, Marcello; Striano, Pasquale; Bagnasco, Irene; Koboldt, Daniel; Iascone, Maria; Suerink, Manon; Kruer, Michael C; Levy, Jonathan; Verloes, Alain; Abbott, Catherine M; Ruaud, Lyse.
Afiliação
  • Paulet A; Département de Génétique, Hôpital Robert-Debré, Paris, France. alix.paulet@hotmail.fr.
  • Bennett-Ness C; Centre for Genomic and Experimental Medicine and Simons Initiative for the Developing Brain, Institute of Genetics and Cancer, Edinburgh, Scotland, UK.
  • Ageorges F; Département de Génétique, Hôpital Robert-Debré, Paris, France.
  • Trost D; Laboratoire Cerba, Saint-Ouen l'Aumône, France.
  • Green A; UCD School of Medicine and Medical Science Consultant in Clinical Genetics, Dublin, Ireland.
  • Goudie D; Regional Genetics Service, NHS Tayside, Dundee, Scotland, UK.
  • Jewell R; Yorkshire Regional Genetics Service, Leeds Teaching Hospitals NHS Trust, Leeds, England, UK.
  • Kraatari-Tiri M; Department of Clinical Genetics, Research unit of Clinical Medicine, Medical Research Center Oulu, Oulu, Finland.
  • Piard J; Oulu University Hospital and University of Oulu, Oulu, Finland.
  • Coubes C; Centre de Génétique Humaine, CHU Besançon, Besançon, France.
  • Lam W; Service de Génétique Médicale, CHU de Montpellier, Montpellier, France.
  • Lynch SA; South-East of Scotland Clinical Genetics Service, General Hospital, Edinburgh, Scotland, UK.
  • Groeschel S; Clinical Genetics, Children's Health Ireland, Dublin, Ireland.
  • Ramond F; Department of Neuropediatrics, University Children's Hospital, Tuebingen, Germany.
  • Fluss J; Service de Génétique, CHU Saint-Etienne - Hôpital Nord, Saint-Etienne, France.
  • Fagerberg C; University Hospitals of Geneva, Geneva, Switzerland.
  • Brasch Andersen C; Department of Clinical Genetics, Odense University Hospital, Odense, Denmark.
  • Varvagiannis K; Human Genetik, Syddansk Universitet, Odense, Denmark.
  • Kleefstra T; Service de Médecine Génétique, Hôpitaux universitaires de Genève, Geneva, Switzerland.
  • Gérard B; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Fradin M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Vitobello A; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
  • Tenconi R; Center of Excellence for Neuropsychiatry, Vincent van Gogh Institute for Psychiatry, Venray, The Netherlands.
  • Denommé-Pichon AS; Molecular Biology, Nouvel Hôpital Civil, Strasbourg, France.
  • Vincent-Devulder A; Service de Génétique Médicale, Hôpital Sud, CHU de Rennes, Rennes, France.
  • Haack T; UMR-Inserm, Génétique des Anomalies du développement, Université de Bourgogne Franche-Comté, Dijon, France.
  • Marsh JA; Servizio di Genetica Medica, Dipartimento di Pediatra, Padova, Italia.
  • Laulund LW; Unité Fonctionnelle Innovation en Diagnostic génomique des maladies rares, FHU-TRANSLAD, CHU Dijon Bourgogne, Dijon, France.
  • Grimmel M; UMR1231 GAD, Inserm - Université Bourgogne-Franche Comté, Dijon, France.
  • Riess A; Génétique Médicale, CHU de Caen, Caen, France.
  • de Boer E; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Padilla-Lopez S; MRC Human Genetics Unit, Western General Hospital, University of Edinburgh, Edinburgh, Scotland, UK.
  • Bakhtiari S; H C Andersen Children's Hospital, Odense University Hospital, Odense, Denmark.
  • Ostendorf A; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Zweier C; Institute of Medical Genetics and Applied Genomics, University of Tübingen, Tübingen, Germany.
  • Smol T; Department of Clinical Genetics, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
  • Willems M; Department of Human Genetics, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Faivre L; Donders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands.
  • Scala M; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Striano P; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Bagnasco I; Steve and Cindy Rasmussen Institute for Genomic Medicine Nationwide Children's Hospital, Colombus, OH, USA.
  • Koboldt D; Department of Pediatrics, The Ohio State University College of Medicine, Colombus, OH, USA.
  • Iascone M; Department of Human Genetics, Inselspital Bern, University of Bern, 3010, Bern, Switzerland.
  • Suerink M; Institute of Human Genetics, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91054, Erlangen, Germany.
  • Kruer MC; University of Lille, EA7364-RADEME, Medical Genetics Institute, Chu Lille, Lille, France.
  • Levy J; Medical Genetic Department for Rare Diseases and Personalized Medicine, Reference Center AD SOOR, AnDDI-RARE, Groupe DI, Inserm U1298, INM, Montpellier University, Montpellier, France.
  • Verloes A; Centre Hospitalier Universitaire de Montpellier, Montpellier, France.
  • Abbott CM; UMR1231 GAD, Inserm, Université de Bourgogne-Franche Comté, Dijon, France.
  • Ruaud L; Centre de Référence Maladies Rares « Anomalies du développement et syndromes malformatifs ¼, Centre de Génétique, FHU-TRANSLAD et Institut GIMI, CHU dijon, Bourgogne, Dijon, France.
Eur J Hum Genet ; 2024 Apr 03.
Article em En | MEDLINE | ID: mdl-38565641
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article