Less severe clinical manifestations in patients with hereditary angioedema with missense C1INH gene mutations

J Allergy Clin Immunol. 2013 Jun;131(6):1708-11. doi: 10.1016/j.jaci.2012.11.015. Epub 2012 Dec 23.
No abstract available

Publication types

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

MeSH terms

  • Adolescent
  • Child
  • Child, Preschool
  • Complement C1 Inactivator Proteins / genetics*
  • Hereditary Angioedema Types I and II / diagnosis*
  • Hereditary Angioedema Types I and II / genetics*
  • Humans
  • Mutation, Missense*
  • Young Adult

Substances

  • Complement C1 Inactivator Proteins