Variants leading to ELAVL2 haploinsufficiency cause a neurodevelopmental disorder with prominent cognitive, behavioral, and neurological features
Marina Boon(Radboud University Nijmegen), Bert BA de Vries(Radboud University Nijmegen), Mireia Coll-Tané(Radboud University Nijmegen), Sarina Schwartzmann(Charité - Universitätsmedizin Berlin), Henrike L. Sczakiel(Humboldt-Universität zu Berlin), Annette Schenck(Radboud University Nijmegen), Marcello Scala(Hospital for Sick Children), Barbara Franke(Radboud University Nijmegen), Marieke Klein(Radboud University Nijmegen), Louise S. Bicknell(University of Otago), Thomas Smol(Université de Lille), Anna Lokchine(Inserm), Jolijn Verseput(Radboud University Nijmegen), Emily Alderman(B.C. Women's Hospital & Health Centre), Meghan R. Mulligan(University of Otago), Peter Kannu(University of Alberta), Nadra Nasser Samra(Bar-Ilan University), Rolph Pfundt(Radboud University Nijmegen), Pleuni Schreurs(Radboud University Nijmegen), Cornelius Boerkoel(B.C. Women's Hospital & Health Centre), Lauren Jeffries(Yale University), Monica Konstantino(Yale University), Jolanda Schieving(Radboud University Nijmegen), Maarten Massink(Utrecht University), Jonathan Lévy(Assistance Publique – Hôpitaux de Paris), Sylvie Jaillard(Inserm), Pasquale Striano(Istituto Giannina Gaslini), Alain Verloes(Assistance Publique – Hôpitaux de Paris), Roseline Caumes(Université de Lille), Renske Oegema(Utrecht University), Taryn Athey(Alberta Health Services), Barbara Šakić(Radboud University Nijmegen), Amber Begtrup, Erica Gerkes(University Medical Center Groningen), Andrea Accogli(Istituto Giannina Gaslini), Sabine Haase(Praxis für Humangenetik Tübingen), Antonella Boni(Ospedale San Bortolo)
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