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CMT2CC associated with NEFH mutations: a predominantly motor neuronopathy

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  • Contributors CP and DP contribution: conception and design of the work, drafting the work, final approval of the version to be published; agreement for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved.

  • Funding The authors have not declared a specific grant for this research from any funding agency in the public, commercial or not-for-profit sectors.

  • Disclaimer CP has no disclosure to report.

  • Competing interests DP declares donations from Pfizer, LAM Therapeutics and Acceleron to support research activities of his research unit; financial support from Pfizer, Alnylam and Kedrion for participation in national and international meetings; participation in the advisory board of Inflectis, Alnylam and Akcea; speaker honorarium from Alnylam.

  • Provenance and peer review Commissioned; internally peer reviewed.

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