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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

Publication history

  • Received July 27, 2021
  • Accepted July 27, 2021
  • First published September 13, 2021.

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