Inherited primary peripheral neuropathies. Molecular genetics and clinical implications of CMT1A and HNPP

JAMA. 1993 Nov 17;270(19):2326-30. doi: 10.1001/jama.270.19.2326.
No abstract available

Publication types

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

MeSH terms

  • Charcot-Marie-Tooth Disease / diagnosis
  • Charcot-Marie-Tooth Disease / genetics*
  • Chromosomes, Human, Pair 17
  • DNA / analysis
  • Gene Deletion
  • Gene Rearrangement
  • Genetic Markers
  • Genetic Testing
  • Humans
  • Molecular Biology
  • Multigene Family
  • Peripheral Nervous System Diseases / diagnosis
  • Peripheral Nervous System Diseases / genetics*
  • Phenotype

Substances

  • Genetic Markers
  • DNA