An axonal form of Charcot-Marie-Tooth disease with a novel missense mutation in the myelin protein zero gene

J Peripher Nerv Syst. 2004 Mar;9(1):1-2. doi: 10.1111/j.1085-9489.2004.09101.x.
No abstract available

Publication types

  • Case Reports
  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Axons / pathology*
  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / pathology
  • Female
  • Humans
  • Mutation, Missense*
  • Myelin P0 Protein / genetics*
  • Polymorphism, Single-Stranded Conformational

Substances

  • Myelin P0 Protein