Two novel mutations in the LOR gene in three families with loricrin keratoderma

Br J Dermatol. 2015 Apr;172(4):1158-62. doi: 10.1111/bjd.13414. Epub 2015 Mar 9.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Female
  • Genes, pX / genetics*
  • Heterozygote
  • Humans
  • Keratoderma, Palmoplantar
  • Male
  • Membrane Proteins / genetics*
  • Middle Aged
  • Skin Diseases, Genetic / genetics*
  • Young Adult

Substances

  • Membrane Proteins
  • loricrin

Supplementary concepts

  • Vohwinkel Syndrome, Variant Form