Identification of a recurrent mitochondrial mutation in a Japanese family with palmoplantar keratoderma, nail dystrophy, and deafness

Eur J Dermatol. 2015 Jan-Feb;25(1):79-81. doi: 10.1684/ejd.2014.2461.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • DNA / genetics*
  • DNA Mutational Analysis
  • Deafness / diagnosis
  • Deafness / genetics*
  • Female
  • Humans
  • Japan
  • Keratoderma, Palmoplantar / diagnosis
  • Keratoderma, Palmoplantar / genetics*
  • Mitochondria / genetics*
  • Mutation*
  • Nails / pathology*
  • Recurrence

Substances

  • DNA