More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation

Pediatr Allergy Immunol. 2021 May;32(4):793-797. doi: 10.1111/pai.13441. Epub 2021 Jan 19.
No abstract available

Publication types

  • Letter

MeSH terms

  • Common Variable Immunodeficiency* / diagnosis
  • Common Variable Immunodeficiency* / genetics
  • Humans
  • Mutation
  • NF-kappa B p52 Subunit / genetics
  • Primary Immunodeficiency Diseases*

Substances

  • NF-kappa B p52 Subunit
  • NFKB2 protein, human