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Case report
Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene

Authors

  • Willem M A Verhoeven Centre of Excellence for Neuropsychiatry, Vincent Van Gogh Institute, Venray, The NetherlandsDepartment of Psychiatry, Erasmus Medical Centre, Rotterdam, The Netherlands PubMed articlesGoogle scholar articles
  • Jos I M Egger Centre of Excellence for Neuropsychiatry, Vincent Van Gogh Institute, Venray, The NetherlandsDonders Institute for Brain, Cognition and Behaviour, Radboud University, Nijmegen, The Netherlands PubMed articlesGoogle scholar articles
  • Paddy K C Janssen Department of Hospital Pharmacy, VieCuri Medical Centre, Venlo, The NetherlandsDepartment of Clinical Pharmacy and Toxicology, Maastricht University Medical Centre, Maastricht, The Netherlands PubMed articlesGoogle scholar articles
  • Arie van Haeringen Department of Clinical Genetics, Leiden University Medical Centre, Leiden, The Netherlands PubMed articlesGoogle scholar articles
  1. Correspondence to Professor Willem M A Verhoeven; wmaverhoeven{at}planet.nl
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Citation

Verhoeven WMA, Egger JIM, Janssen PKC, et al
Adult male patient with severe intellectual disability caused by a homozygous mutation in the HNMT gene

Publication history

  • Accepted September 28, 2020
  • First published December 12, 2020.
Online issue publication 
December 12, 2020

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