Pathogenic NFKB2 variant in the ankyrin repeat domain (R635X) causes a variable antibody deficiency

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

Abstract

Metadata

Authors/Creators:
  • Tuijnenburg, P
  • Allen, HL
  • de Bree, GJ
  • Savic, S ORCID logo https://orcid.org/0000-0001-7910-0554
  • Jansen, MH
  • Stockdale, C
  • Simeoni, I
  • Ten Berge, IJM
  • van Leeuwen, EMM
  • BioResource, NIHR
  • Thaventiran, JE
  • Kuijpers, TW
Copyright, Publisher and Additional Information: (c) 2019, The Authors. Published by Elsevier Inc. This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).
Keywords: Common variable immunodeficiency; NFKB2; B cells; T cells
Dates:
  • Accepted: 27 March 2019
  • Published (online): 3 April 2019
  • Published: June 2019
Institution: The University of Leeds
Academic Units: The University of Leeds > Faculty of Medicine and Health (Leeds) > School of Medicine (Leeds) > Institute of Rheumatology & Musculoskeletal Medicine (LIRMM) (Leeds)
Depositing User: Symplectic Publications
Date Deposited: 25 Apr 2019 08:21
Last Modified: 25 Apr 2019 08:21
Status: Published
Publisher: Elsevier
Identification Number: https://doi.org/10.1016/j.clim.2019.03.010
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