A novel NTRK1 mutation associated with congenital insensitivity to pain with anhidrosis

Am J Hum Genet. 1999 Apr;64(4):1207-10. doi: 10.1086/302319.
No abstract available

Publication types

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

MeSH terms

  • 3T3 Cells
  • Amino Acid Substitution / genetics
  • Animals
  • Base Sequence
  • Exons / genetics
  • Female
  • Hereditary Sensory and Autonomic Neuropathies / genetics*
  • Humans
  • Male
  • Mice
  • Pedigree
  • Point Mutation / genetics*
  • Receptor, trkA / chemistry
  • Receptor, trkA / genetics*
  • Receptor, trkA / metabolism

Substances

  • Receptor, trkA

Grants and funding