Novel keratin 14 mutations in patients with severe recessive epidermolysis bullosa simplex

J Invest Dermatol. 2006 Aug;126(8):1912-4. doi: 10.1038/sj.jid.5700312. Epub 2006 Apr 13.
No abstract available

Publication types

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

MeSH terms

  • Child, Preschool
  • Epidermolysis Bullosa Simplex / genetics*
  • Genes, Recessive
  • Humans
  • Keratin-14
  • Keratins / genetics*
  • Male
  • Point Mutation*
  • Severity of Illness Index

Substances

  • KRT14 protein, human
  • Keratin-14
  • Keratins