Transcriptomic analysis of skin in a case of ichthyosis Curth-Macklin caused by a KRT1 mutation

Br J Dermatol. 2016 Dec;175(6):1372-1375. doi: 10.1111/bjd.14969. Epub 2016 Oct 23.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Dermatitis, Seborrheic / genetics*
  • Female
  • Gene Expression Profiling
  • Homozygote
  • Humans
  • Ichthyosis / genetics*
  • Keratin-1 / genetics*
  • Mutation / genetics*

Substances

  • KRT1 protein, human
  • Keratin-1

Supplementary concepts

  • Ichthyosis hystrix, Curth Macklin type