Coexistence of KRT14 and KRT5 mutations in a Polish patient with epidermolysis bullosa simplex

Br J Dermatol. 2014 Feb;170(2):468-9. doi: 10.1111/bjd.12624.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Child, Preschool
  • Epidermolysis Bullosa Simplex / genetics*
  • Humans
  • Keratin-14 / genetics*
  • Keratin-5 / genetics*
  • Male
  • Mutation / genetics*
  • Pedigree

Substances

  • Keratin-14
  • Keratin-5