Bi-allelic PRMT9 loss-of-function variants cause a syndromic form of intellectual disability

Ariane Kröll‐Hermi(Inserm), Olivier Kassel(Karlsruhe Institute of Technology), Kimia Kahrizi(University of Social Welfare and Rehabilitation Sciences), Jonathan Lévy(Assistance Publique – Hôpitaux de Paris), Tatjana Bierhals(Universität Hamburg), Levon Halabelian(University of Toronto), Saskia B. Wortmann(Paracelsus Medical University), Ingrid M. Wentzensen, Lev Grinstein(Universität Hamburg), Sophie Scheidecker(Inserm), Amélie Piton(Centre National de la Recherche Scientifique), Kristian Tveten(Telemark Hospital), Élise Schaefer(Pennsylvania State University), Teresa Santiago‐Sim(Baylor Genetics), Francesca Mattioli(Centre National de la Recherche Scientifique), Marie Falkenberg Smeland(University Hospital of North Norway), Claire Feger(Hôpitaux Universitaires de Strasbourg), Anne‐Claude Tabet(Assistance Publique – Hôpitaux de Paris), Cathy Obringer(Inserm), Matheus Augusto Araújo Castro(Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo), Megana Prasad(Inserm), Laurie Ruch(Inserm), Véronique Geoffroy(Génétique Médicale & Génomique Fonctionelle), Corinne Stoetzel(Inserm), Céline Keime(Centre National de la Recherche Scientifique), Blandine Dozières(Assistance Publique – Hôpitaux de Paris), Antje Kampmeier(University of Duisburg-Essen), Chumei Li(McMaster University Medical Centre), Lyse Ruaud(Inserm), René G. Feichtinger(Paracelsus Medical University), Johannes A. Mayr(Paracelsus Medical University), Anna Ruiz(Universitat Autònoma de Barcelona), Christelle Etard(Kerntechnische Entsorgung Karlsruhe (Germany)), Hernán Gonorazky(Hospital Italiano de Buenos Aires), Elisabeth Gabau(Universitat Autònoma de Barcelona), Hong Zeng(Kunming Institute of Botany), Naomichi Matsumoto(Yokohama City University), Theresia Herget(Universität Hamburg), Xiaodong Wang(Shanghai Children's Medical Center), Jia Wang(Cipher Gene (China)), Chong Ae Kim(AstraZeneca (United States)), Fengling Li(University of Toronto), Atsushi Fujita(Yokohama City University), Roman Yusupov(Joe DiMaggio Children's Hospital), Jamali Payman(University of Social Welfare and Rehabilitation Sciences), Damien Plassard(Centre National de la Recherche Scientifique), Gina Cowing(McMaster University Medical Centre), Ebba Alkhunaizi(University of Toronto)
The American Journal of Human Genetics
November 18, 2025
Cited by 1


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