A novel point mutation in the keratin 17 gene in a Japanese case of pachyonychia congenita type 2

J Invest Dermatol. 2002 Mar;118(3):545-7. doi: 10.1046/j.0022-202x.2001.01701.x.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Asian People / genetics
  • Cysts / genetics*
  • Hair / abnormalities*
  • Humans
  • Japan
  • Keratins / genetics*
  • Keratoderma, Palmoplantar / genetics*
  • Male
  • Nail Diseases / genetics*
  • Point Mutation*
  • Skin Diseases / genetics*

Substances

  • Keratins