N98S mutation in NEFL gene is dominantly inherited with a phenotype of polyneuropathy and cerebellar atrophy

Yi Yang, Li Qiang Gu, William B. Burnette, Jun Li

Research output: Contribution to journalLetterpeer-review

13 Scopus citations
Original languageEnglish (US)
Pages (from-to)46-47
Number of pages2
JournalJournal of the Neurological Sciences
Volume365
DOIs
StatePublished - Jun 15 2016

Keywords

  • Axonal loss
  • Cerebellar atrophy
  • Charcot-Marie-Tooth disease
  • Dysmyelination
  • Myelin
  • NEFL
  • Nerve conduction study

ASJC Scopus subject areas

  • Neurology
  • Clinical Neurology

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