Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b

J Dermatol. 2014 Jan;41(1):108-9. doi: 10.1111/1346-8138.12349. Epub 2013 Dec 20.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Age of Onset
  • Child
  • Female
  • Humans
  • Keratin-6 / genetics*
  • Mutation, Missense
  • Pachyonychia Congenita / genetics*
  • Protein Structure, Tertiary

Substances

  • KRT6B protein, human
  • Keratin-6