The Kindler syndrome: a spectrum of FERMT1 mutations in Iranian families

J Invest Dermatol. 2015 May;135(5):1447-1450. doi: 10.1038/jid.2015.9. Epub 2015 Jan 19.
No abstract available

Publication types

  • Letter

MeSH terms

  • Blister / diagnosis
  • Blister / ethnology*
  • Blister / genetics*
  • Epidermolysis Bullosa / diagnosis
  • Epidermolysis Bullosa / ethnology*
  • Epidermolysis Bullosa / genetics*
  • Female
  • Heterozygote
  • Homozygote
  • Humans
  • Iran
  • Male
  • Membrane Proteins / genetics*
  • Mutation / genetics*
  • Neoplasm Proteins / genetics*
  • Pedigree
  • Periodontal Diseases / diagnosis
  • Periodontal Diseases / ethnology*
  • Periodontal Diseases / genetics*
  • Photosensitivity Disorders / diagnosis
  • Photosensitivity Disorders / ethnology*
  • Photosensitivity Disorders / genetics*
  • Prenatal Diagnosis

Substances

  • FERMT1 protein, human
  • Membrane Proteins
  • Neoplasm Proteins

Supplementary concepts

  • Poikiloderma of Kindler