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

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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