Novel mutation (p.L91P, c.272T>C) of keratin 17 in a case with pachyonychia congenita type 2

J Dermatol. 2013 Sep;40(9):757-8. doi: 10.1111/1346-8138.12212. Epub 2013 Jul 16.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • Female
  • Humans
  • Keratin-17 / genetics*
  • Pachyonychia Congenita / genetics*

Substances

  • Keratin-17