The CNS phenotype of X-linked Charcot-Marie-Tooth disease: more than a peripheral problem

Neurology. 2003 Dec 9;61(11):1475-8. doi: 10.1212/01.wnl.0000095960.48964.25.
No abstract available

Publication types

  • Case Reports

MeSH terms

  • Brain / pathology
  • Central Nervous System Diseases / genetics
  • Charcot-Marie-Tooth Disease / diagnosis*
  • Charcot-Marie-Tooth Disease / genetics
  • Child
  • Connexins / genetics
  • Demyelinating Diseases / diagnosis*
  • Encephalomyelitis / diagnosis*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Phenotype

Substances

  • Connexins
  • connexin 32