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Mutations in NSUN2 cause autosomal-recessive intellectual disability
Authors:Abbasi-Moheb Lia  Mertel Sara  Gonsior Melanie  Nouri-Vahid Leyla  Kahrizi Kimia  Cirak Sebahattin  Wieczorek Dagmar  Motazacker M Mahdi  Esmaeeli-Nieh Sahar  Cremer Kirsten  Weißmann Robert  Tzschach Andreas  Garshasbi Masoud  Abedini Seyedeh S  Najmabadi Hossein  Ropers H Hilger  Sigrist Stephan J  Kuss Andreas W
Institution:1. Max Planck Institute for Molecular Genetics, Ihnestraße 73, D-14195 Berlin, Germany;2. Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran 1985713834, Iran;3. Institute for Biology/Genetics, Freie Universität Berlin, Takustraße 6, D-14195 Berlin, Germany;4. Great Ormond Street Children''s Hospital, Institute of Child Health, 30 Guilford Street, London WC1N1EH, UK;5. Institut für Humangenetik, Universitätsklinikum, Hufelandstraße 55, D-45147 Essen, Germany;6. Institute for Human Genetics, University Medicine Greifswald & Interfaculty Institute for Genetics and Functional Genomics, Ernst Moritz Arndt University, Greifswald, Fleischmannstraße 42–44, D-17489 Greifswald, Germany;7. NeuroCure Cluster of Excellence, Charité, Charitéplatz 1, D-10117 Berlin, Germany
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