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Editorial
. 2018 Oct;142(4):1062-1065.
doi: 10.1016/j.jaci.2018.06.050. Epub 2018 Aug 28.

Nuclear factor κB mutations in human subjects: The devil is in the details

Manfred Fliegauf  1 , Bodo Grimbacher  2
Affiliations
Editorial

Nuclear factor κB mutations in human subjects: The devil is in the details

Manfred Fliegauf et al. J Allergy Clin Immunol. 2018 Oct.
No abstract available

Keywords: NFKB1; common variable immunodeficiency; nuclear factor κB signaling; primary immunodeficiency disease.

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  • Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.
    Tuijnenburg P, Lango Allen H, Burns SO, Greene D, Jansen MH, Staples E, Stephens J, Carss KJ, Biasci D, Baxendale H, Thomas M, Chandra A, Kiani-Alikhan S, Longhurst HJ, Seneviratne SL, Oksenhendler E, Simeoni I, de Bree GJ, Tool ATJ, van Leeuwen EMM, Ebberink EHTM, Meijer AB, Tuna S, Whitehorn D, Brown M, Turro E, Thrasher AJ, Smith KGC, Thaventhiran JE, Kuijpers TW; NIHR BioResource–Rare Diseases Consortium. Tuijnenburg P, et al. J Allergy Clin Immunol. 2018 Oct;142(4):1285-1296. doi: 10.1016/j.jaci.2018.01.039. Epub 2018 Mar 2. J Allergy Clin Immunol. 2018. PMID: 29477724 Free PMC article.

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