Charcot-Marie-Tooth disease due to the Thr124Met mutation in the myelin protein zero gene associated with multiple sclerosis

J Peripher Nerv Syst. 2005 Dec;10(4):388-9. doi: 10.1111/j.1085-9489.2005.00054.x.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Charcot-Marie-Tooth Disease / complications
  • Charcot-Marie-Tooth Disease / genetics*
  • Female
  • Humans
  • Methionine / genetics*
  • Middle Aged
  • Multiple Sclerosis / complications
  • Multiple Sclerosis / genetics*
  • Mutation*
  • Myelin P0 Protein / genetics*
  • Threonine / genetics*

Substances

  • Myelin P0 Protein
  • Threonine
  • Methionine