Molecular genetics of Charcot-Marie-Tooth neuropathy

Adv Hum Genet. 1994:22:117-52. doi: 10.1007/978-1-4757-9062-7_3.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.
  • Review

MeSH terms

  • Charcot-Marie-Tooth Disease / genetics*
  • Charcot-Marie-Tooth Disease / pathology
  • Charcot-Marie-Tooth Disease / physiopathology
  • Chromosome Deletion
  • Chromosome Mapping
  • Chromosomes, Human, Pair 17
  • Female
  • Humans
  • Male
  • Multigene Family
  • Myelin Proteins / genetics
  • Pedigree
  • Peripheral Nerves / physiology
  • Peripheral Nerves / physiopathology
  • Recombination, Genetic

Substances

  • Myelin Proteins
  • PMP22 protein, human