Mutations in NSUN2 Cause Autosomal- Recessive Intellectual Disability
Lia Abbasi‐Moheb(Max Planck Institute for Molecular Genetics), Sara Mertel(Freie Universität Berlin), Melanie Gonsior(Freie Universität Berlin), Leyla Nouri-Vahid(University of Social Welfare and Rehabilitation Sciences), Kimia Kahrizi(University of Social Welfare and Rehabilitation Sciences), Sebahattin Çirak(Great Ormond Street Hospital), Dagmar Wieczorek, Mohammad Mahdi Motazacker(Max Planck Institute for Molecular Genetics), Sahar Esmaeeli-Nieh(Max Planck Institute for Molecular Genetics), Kirsten Cremer, Robert Weißmann(Universität Greifswald), Andreas Tzschach(Max Planck Institute for Molecular Genetics), Masoud Garshasbi(Max Planck Institute for Molecular Genetics), Seyedeh Sedigheh Abedini(University of Social Welfare and Rehabilitation Sciences), Hossein Najmabadi(University of Social Welfare and Rehabilitation Sciences), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Stephan J. Sigrist(Freie Universität Berlin), Andreas W. Kuß(Max Planck Institute for Molecular Genetics)
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