Recurrent KIND1 (C20orf42) gene mutation, c.676insC, in a Brazilian pedigree with Kindler syndrome

Br J Dermatol. 2007 Dec;157(6):1281-4. doi: 10.1111/j.1365-2133.2007.08219.x. Epub 2007 Oct 4.
No abstract available

Publication types

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

MeSH terms

  • Female
  • Genetic Carrier Screening
  • Humans
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Neoplasm Proteins / genetics*
  • Pedigree
  • Skin Diseases, Genetic / genetics*
  • Syndrome

Substances

  • FERMT1 protein, human
  • Membrane Proteins
  • Neoplasm Proteins