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Editorial commentary
CMT2CC associated with NEFH mutations: a predominantly motor neuronopathy

Authors

  • Chiara Pisciotta Rare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy PubMed articlesGoogle scholar articles
  • Davide Pareyson Rare Neurodegenerative and Neurometabolic Diseases Unit, Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano, Italy PubMed articlesGoogle scholar articles
  1. Correspondence to Dr Davide Pareyson, Rare Neurodegenerative and Neurometabolic Diseases Unit - Department of Clinical Neurosciences, Fondazione IRCCS Istituto Neurologico Carlo Besta, Milano 20133 Lombardia, Italy; davide.pareyson{at}istituto-besta.it
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Citation

Pisciotta C, Pareyson D
CMT2CC associated with NEFH mutations: a predominantly motor neuronopathy
Journal of Neurology, Neurosurgery & Psychiatry 2022;93:1.

Publication history

  • Received July 27, 2021
  • Accepted July 27, 2021
  • First published September 13, 2021.
Online issue publication 
July 06, 2022

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© Author(s) (or their employer(s)) 2022. No commercial re-use. See rights and permissions. Published by BMJ.