Novel mutation of the myelin P0 gene in a CMT1B family

Hum Mutat. 1997;9(1):74-7. doi: 10.1002/(SICI)1098-1004(1997)9:1<74::AID-HUMU16>3.0.CO;2-M.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Arginine / genetics
  • Charcot-Marie-Tooth Disease / genetics*
  • Female
  • Genes, Dominant
  • Histidine / genetics
  • Humans
  • Male
  • Mutation*
  • Myelin Proteins / genetics*
  • Pedigree

Substances

  • Myelin Proteins
  • Histidine
  • Arginine