The Pro162 variant is a loss-of-function mutation of the human melanocortin 1 receptor gene

J Invest Dermatol. 2001 Jul;117(1):156-8. doi: 10.1046/j.0022-202x.2001.01393.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Animals
  • Humans
  • Melanoma / genetics*
  • Point Mutation*
  • Receptors, Corticotropin / genetics*
  • Receptors, Melanocortin
  • Skin Neoplasms / genetics*
  • Tumor Cells, Cultured

Substances

  • Receptors, Corticotropin
  • Receptors, Melanocortin