Bi-allelic variants in FSD1L cause a neurodevelopmental disorder overlapping with L1 syndrome
Valentina Serpieri(University of Pavia), Enza Maria Valente(University of Pavia), Laurent Hermitte(Aix-Marseille Université), Bruno J. Gonzalez(Inserm), Noor Smal(VIB-UAntwerp Center for Molecular Neurology), Grace Rabie(Bethlehem University), Alice M. H. Bedois(Eurofins (France)), Florent Marguet(Inserm), Alessia Micalizzi(University of Messina), Moien Kanaan(Diyarbakır Askeri Hastanesi), François Janin(Inserm), C Mazzotta(University of Pavia), Claudia Condoluci, Simone Sabbioneda(Istituto di Genetica Molecolare), Francesco Petrizzelli(Casa Sollievo della Sofferenza), Monia Ginevrino(University of Pavia), Maryline Lecointre(Inserm), Silvia Bione(Istituto di Genetica Molecolare), Anna Garbelli(Istituto di Genetica Molecolare), Alessia Orsi(University of Pavia), Myriam Vezain-Mouchard(Inserm), Roberta De Mori(University of Messina), Annie Laquerrière(Inserm), Tommaso Mazza(Agostino Gemelli University Polyclinic), Pascale Marcorelles(Centre Hospitalier Régional Universitaire de Brest), Carla Marini(Ospedali Riuniti Umberto I), Valentin Ruault(Centre Hospitalier Universitaire de Montpellier), Gaël Nicolas(Inserm), Pascale Saugier-Veber(Inserm), Frederic Tran-Mau-Them(Inserm), Sarah Weckhuysen(VIB-UAntwerp Center for Molecular Neurology), Anna Pichiecchio(University of Pavia), Béatrice Desnous(Inserm), Alice Goldenberg(Inserm), Nathalie Drouot(Centre National de la Recherche Scientifique)
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