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Article

Tuijnenburg, P, Allen, HL, de Bree, GJ et al. (9 more authors) (2019) Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency. Clinical Immunology, 203. pp. 23-27. ISSN 1521-6616

Wei, W, Tuna, S, Keogh, MJ et al. (426 more authors) (2019) Germline selection shapes human mitochondrial DNA diversity. Science, 364 (6442). 749-+. ISSN 0036-8075

Tuijnenburg, P, Lango Allen, H, Burns, SO et al. (28 more authors) (2018) Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans. Journal of Allergy and Clinical Immunology, 142 (4). pp. 1285-1296. ISSN 0091-6749

Lawless, D, Geier, CB, Farmer, JR et al. (43 more authors) (2018) Prevalence and clinical challenges among adults with primary immunodeficiency and recombination-activating gene deficiency. Journal of Allergy and Clinical Immunology, 141 (6). pp. 2303-2306. ISSN 0091-6749

This list was generated on Sun Oct 13 17:19:26 2019 BST.