Charcot-Marie-Tooth disease type 2 and P0 gene mutations

Neurology. 1999 Mar 23;52(5):1110-1. doi: 10.1212/wnl.52.5.1106-f.
No abstract available

Publication types

  • Case Reports
  • Comment
  • Letter

MeSH terms

  • Adult
  • Charcot-Marie-Tooth Disease / genetics*
  • Female
  • Humans
  • Mutation
  • Myelin P0 Protein / genetics*
  • Phenotype

Substances

  • Myelin P0 Protein

Grants and funding