A novel complex insertion-deletion mutation in ADAR1 gene in a Chinese family with dyschromatosis symmetrica hereditaria

J Eur Acad Dermatol Venereol. 2011 Jun;25(6):743-6. doi: 10.1111/j.1468-3083.2010.03773.x. Epub 2010 Jun 25.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Asian People / genetics
  • Family Health*
  • Female
  • Humans
  • Mutagenesis, Insertional
  • Pigmentation Disorders / congenital*
  • Pigmentation Disorders / genetics
  • Sequence Analysis, DNA
  • Sequence Deletion

Supplementary concepts

  • Dyschromatosis symmetrica hereditaria 1