Two cases of Marie Unna hereditary hypotrichosis: clinical features and mutation analysis of the U2HR and EPS8L3 genes

Clin Exp Dermatol. 2014 Mar;39(2):225-7. doi: 10.1111/ced.12245. Epub 2013 Nov 16.
No abstract available

Publication types

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

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics*
  • Adolescent
  • Adult
  • Female
  • Humans
  • Hypotrichosis / congenital*
  • Hypotrichosis / genetics
  • Male
  • Mutation*
  • Transcription Factors / genetics*

Substances

  • Adaptor Proteins, Signal Transducing
  • EPS8L3 protein, human
  • HR protein, human
  • Transcription Factors