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

Subjects

Subjects :

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

Details

Language :

English

ISSN :

1399-3038

Volume :

32

Issue :

4

Database :

MEDLINE

Journal :

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology

Publication Type :

Editorial & Opinion

Accession number :

33369776

Full Text :

https://doi.org/10.1111/pai.13441