Article info

Letter
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP

Authors

  1. Correspondence to Dr Olaf Ansorge, Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX1 2JD, UK; olaf.ansorge{at}ndcn.ox.ac.uk
View Full Text

Citation

Nolan M, Barbagallo P, Turner MR, et al
Isolated homozygous R217X OPTN mutation causes knock-out of functional C-terminal optineurin domains and associated oligodendrogliopathy-dominant ALS–TDP

Publication history

  • Received December 14, 2020
  • Revised January 28, 2021
  • Accepted February 2, 2021
  • First published March 16, 2021.
Online issue publication 
August 13, 2021

Article Versions

  • Supplementary Data

    This web only file has been produced by the BMJ Publishing Group from an electronic file supplied by the author(s) and has not been edited for content.

Request permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.