Associated Papers
Compound heterozygous NFKB1 missense variants in cis associated with immunodeficiency.
Fliegauf M et al.
Clinical Immunology (orlando, Fla.), 2026
Detrimental NFKB1 missense variants affecting the Rel-homology domain of p105/p50.
Fliegauf M et al.
Frontiers in Immunology, 2022
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J et al.
The Journal of Experimental Medicine, 2021
Select a paper to view details