Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)

Paulet A, Bennett-Ness C, Ageorges F, Trost D, Green A, Goudie D, Jewell R, Kraatari-Tiri M, PIARD J, Coubes C, Lam W, Lynch SA, Groeschel S, Ramond F, Fluss J, Fagerberg C, Brasch Andersen C, Varvagiannis K, Kleefstra T, Gérard B, Fradin M, Vitobello A, Tenconi R, Denommé-Pichon AS, Vincent-Devulder A, Haack T, Marsh JA, Laulund LW, Grimmel M, Riess A, de Boer E, Padilla-Lopez S, Bakhtiari S, Ostendorf A, Zweier C, Smol T, Willems M, Faivre L, Scala M, Striano P, Bagnasco I, Koboldt D, Iascone M, Suerink M, Kruer MC, Levy J, Verloes A, Abbott CM, Ruaud L (2024)


Publication Type: Journal article, Erratum

Publication year: 2024

Journal

DOI: 10.1038/s41431-024-01606-x

Abstract

Correction to: European Journal of Human Geneticshttps://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.

Involved external institutions

Hôpital Universitaire Robert-Debré FR France (FR) Laboratoire CERBA FR France (FR) University College Dublin (UCD) IE Ireland (IE) NHS Lothian GB United Kingdom (GB) Temple Street Children's University Hospital / Children's Health Ireland (CHI) IE Ireland (IE) Universitätsklinikum Tübingen DE Germany (DE) University of Edinburgh GB United Kingdom (GB) Centre Hospitalier Universitaire de Saint-Étienne (CHU) FR France (FR) Geneva University Hospitals / Hôpitaux universitaires de Genève (HUG) CH Switzerland (CH) Odense Universitetshospital (OUH) DK Denmark (DK) Eberhard Karls Universität Tübingen DE Germany (DE) Barrow Neurological Institute US United States (USA) (US) Erasmus University Medical Center (MC) NL Netherlands (NL) NHS Tayside GB United Kingdom (GB) Leeds Teaching Hospitals NHS Trust GB United Kingdom (GB) Oulun Yliopisto / University of Oulo FI Finland (FI) University of Southern Denmark / Syddansk Universitet DK Denmark (DK) Université de Strasbourg (UDS) FR France (FR) Centre hospitalier universitaire de Rennes / CHU Rennes FR France (FR) Université Bourgogne Franche-Comté FR France (FR) Centre hospitalier universitaire (CHU) de Dijon Bourgogne FR France (FR) CHU de Caen Normandie FR France (FR) Centre hospitalier régional et universitaire de Besançon (CHRU Besancon) FR France (FR) Centre Hospitalier Universitaire de Montpellier (CHU/CHRU MTP) FR France (FR) Nationwide Children's Hospital US United States (USA) (US) Inselspital, Universitätsspital Bern CH Switzerland (CH) Istituto Giannina Gaslini IT Italy (IT) Université de Lille (ULille) / University of Lille Nord de France / Université Lille Nord de France / Université Lille II FR France (FR) Martini Ziekenhuis NL Netherlands (NL) A.S.L. Napoli 1 Centro IT Italy (IT) Leiden University Medical Center NL Netherlands (NL) Institute for Neurosciences of Montpellier (INM) FR France (FR)

How to cite

APA:

Paulet, A., Bennett-Ness, C., Ageorges, F., Trost, D., Green, A., Goudie, D.,... Ruaud, L. (2024). Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8). European Journal of Human Genetics. https://doi.org/10.1038/s41431-024-01606-x

MLA:

Paulet, Alix, et al. "Correction to: Expansion of the neurodevelopmental phenotype of individuals with EEF1A2 variants and genotype-phenotype study (European Journal of Human Genetics, (2024), 10.1038/s41431-024-01560-8)." European Journal of Human Genetics (2024).

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