A de novo COL17A1 splice-site mutation causing a 7-bp deletion in a Taiwanese patient with junctional epidermolysis bullosa

Eur J Dermatol. 2021 Apr 1;31(2):267-269. doi: 10.1684/ejd.2021.4011.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • Autoantigens / genetics*
  • Collagen Type XVII
  • Epidermolysis Bullosa, Junctional / diagnosis
  • Epidermolysis Bullosa, Junctional / genetics*
  • Epidermolysis Bullosa, Junctional / pathology*
  • Humans
  • Male
  • Non-Fibrillar Collagens / genetics*
  • Pedigree
  • RNA Splice Sites
  • Sequence Deletion
  • Taiwan

Substances

  • Autoantigens
  • Non-Fibrillar Collagens
  • RNA Splice Sites