Article info

Original research
Charcot-Marie-Tooth disease type 2CC due to NEFH variants causes a progressive, non-length-dependent, motor-predominant phenotype

Authors

  1. Correspondence to Professor Mary M Reilly, Centre for Neuromuscular Diseases, UCL Queen Square Institute of Neurology, London, UK; m.reilly{at}ucl.ac.uk
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Citation

Pipis M, Cortese A, Polke JM, et al
Charcot-Marie-Tooth disease type 2CC due to NEFH variants causes a progressive, non-length-dependent, motor-predominant phenotype

Publication history

  • Received May 24, 2021
  • Accepted August 8, 2021
  • First published September 13, 2021.
  • 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.

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