Associated Papers
A novel NFKB1 variant in a Japanese pedigree with common variable immunodeficiency.
Nakatani N et al.
Human Genome Variation, 2024
Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
Li J et al.
The Journal of Experimental Medicine, 2021
Keeping it in the family: the case for considering late-onset combined immunodeficiency a subset of common variable immunodeficiency disorders.
Ameratunga R et al.
Expert Review of Clinical Immunology, 2018
Damaging heterozygous mutations in NFKB1 lead to diverse immunologic phenotypes.
Kaustio M et al.
The Journal of Allergy and Clinical Immunology, 2017
Human NF-κB1 Haploinsufficiency and Epstein-Barr Virus-Induced Disease-Molecular Mechanisms and Consequences.
Hoeger B et al.
Frontiers in Immunology, 2017
Haploinsufficiency of the NF-κB1 Subunit p50 in Common Variable Immunodeficiency.
Fliegauf M et al.
American Journal of Human Genetics, 2015
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