First report of a FXII gene mutation in a Brazilian family with hereditary angio-oedema with normal C1 inhibitor

Br J Dermatol. 2015 Oct;173(4):1102-4. doi: 10.1111/bjd.13791. Epub 2015 Sep 1.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Angioedemas, Hereditary / genetics*
  • Complement C1 Inactivator Proteins / genetics
  • Complement C1 Inhibitor Protein
  • Factor XII / genetics*
  • Female
  • Humans
  • Mutation / genetics*
  • Pedigree

Substances

  • Complement C1 Inactivator Proteins
  • Complement C1 Inhibitor Protein
  • SERPING1 protein, human
  • Factor XII