Biochemically deleterious human NFKB1 variants underlie an autosomal dominant form of common variable immunodeficiency.

J Exp Med · 2021 · PMC8421261 · PMID 34473196

Europe PMC DOI

hedged sentence

0.0000

closest p · 0.0× alpha

0.0000

boldest claim

The sentences

highly significantP = 2.78 × 10 −15actually significant

The enrichment in deleterious NFKB1 variants of patients with CVID was selective and highly significant (P = 2.78 × 10 −15 ).

also in 132,142 other papers

Quoted from the open-access full text in Europe PMC under the licence the publisher applied. The sentence is reproduced exactly as published; the emphasis is ours.