Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability

Abolfazl Heidari, Chanakan Tongsook, Reza Najafipour, Luciana Musante, Nasim Vasli, Masoud Garshasbi, Hao Hu, Kirti Mittal, Amy J.M. McNaughton, Kumudesh Sritharan, Melissa Hudson, Henning Stehr, Saeid Talebi, Mohammad Moradi, Hossein Darvish, Muhammad Arshad Rafiq, Hossein Mozhdehipanah, Ali Rashidinejad, Shahram Samiei, Mohsen GhadamiChristian Windpassinger, Gabriele Gillessen-Kaesbach, Andreas Tzschach, Iltaf Ahmed, Anna Mikhailov, D. James Stavropoulos, Melissa T. Carter, Soraya Keshavarz, Muhammad Ayub, Hossein Najmabadi, Xudong Liu, Hans Hilger Ropers, Peter Macheroux, John B. Vincent^*

^*Korrespondierende/r Autor/-in für diese Arbeit

Institut für Humangenetik

Centre for Addiction and Mental Health
MPI Molekulare Genetik
Tarbiat Modares University
Stanford University
Tehran University of Medical Sciences
Shahid Beheshti University of Medical Sciences
Qazvin University of Medical Sciences
Iranian Blood Transfusion Organization
Medical University Graz
Technische Universität Dresden
National University of Sciences and Technology (NUST)
The Hospital for Sick Children
Queen's University, Kingston
University of Social Welfare and Rehabilitation Sciences
University Health Network

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Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability

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Biochemistry, Genetics and Molecular Biology