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

Abolfazl Heidari, Chanakan Tongsook, Reza Najafipour, Luciana Musante, Nasium Vasli, Masoud Garshasbi, Hao Hu, Kirti Mittal, Amy McNaughton, Kumudesh Sritharan, Melissa Hudson, Henning Stehr, Saeid Talebi, Mohammad Moradi, Hossein Darvish, Muhammad Arshad Rafiq, Hossein Mozhdehipanah, Christian Windpassinger, Gabriele Gillessen-Kaesbach, Andreas TzschachIltaf Ahmed, Anna Mikhailov, James Stavropoulos, Melissa Carter, Soraya Keshavarz, Muhammad Ayub, Hossein Najmabadi, Xudong Liu, Hans Hilger Ropers, Peter Macheroux, John Vincent

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)5697-5710
JournalHuman molecular genetics
Volume24
Issue number20
Publication statusPublished - 2015

Fields of Expertise

  • Human- & Biotechnology

Treatment code (Nähere Zuordnung)

  • Basic - Fundamental (Grundlagenforschung)

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