Mutations in the histamine<i>N</i>-methyltransferase gene,<i>HNMT</i>, are associated with nonsyndromic autosomal recessive intellectual disability
Abolfazl Heidari(Hospital for Sick Children), John B. Vincent(Centre for Addiction and Mental Health), Masoud Garshasbi(Max Planck Institute for Molecular Genetics), Kirti Mittal(Centre for Addiction and Mental Health), Luciana Musante(IRCCS Materno Infantile Burlo Garofolo), Chanakan Tongsook(Graz University of Technology), S Keshavarz(Cellular Research (United States)), Muhammad Rafiq(Centre for Addiction and Mental Health), Hossein Mozhdehipanah(Sina Hospital), Reza Najafipour(University of Social Welfare and Rehabilitation Sciences), Hao Hu(Chengdu Sport University), Dimitrios J. Stavropoulos(Hospital for Sick Children), Henning Stehr(Stanford University), Christian Windpassinger(Medical University of Graz), Kumudesh Sritharan(Centre for Addiction and Mental Health), Muhammad Ayub(King's College London), Hossein Najmabadi(Yahoo (Spain)), Amy J. M. McNaughton(Ontario Genomics), Andreas Tzschach(Max Planck Institute for Molecular Genetics), Ali Rashidinejad(Riddet Institute), Melissa T. Carter(Agricultural Research Institute of Ontario), Peter Macheroux(Graz University of Technology), Melissa M. Hudson(Cincinnati Children's Hospital Medical Center), Xudong Liu(Queen's University), Mohammad Moradi(Cellular Research (United States)), Hossein Darvish(University of Social Welfare and Rehabilitation Sciences), Anna Mikhailov(Centre for Addiction and Mental Health), Hans Hilger Ropers(Max Planck Institute for Molecular Genetics), Shahram Samiei(High Institute for Education and Research in Transfusion Medicine), Gabriele Gillessen‐Kaesbach(University Hospital Schleswig-Holstein), Nasim Vasli(Centre National de la Recherche Scientifique), Iltaf Ahmed(Centre for Addiction and Mental Health), Mohsen Ghadami(Tehran University of Medical Sciences)
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