Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.
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J Exp Med. 2021 Nov 1;218(11):e20210566. doi: 10.1084/jem.20210566. Epub 2021 Sep 2.
J Exp Med. 2021.
PMID: 34473196
Free PMC article.