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

Author(s):: Verhoeven, W.M.A.; Egger, J.I.M.; Janssen, P.K.C.; Haeringen, A. van (0000-0003-3786-6716)

Published: 2020
Publication type: Article / Letter to editor

Date issued: 2020-12-12
Language: English
Publisher: BMJ Publishing Group
Is part of: BMJ Case Reports
hdl: 1887/3196040
doi: 10.1136/bcr-2020-235972
URL: https://casereports.bmj.com/content/13/12/e235972.info