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Loss-of-function nuclear factor κB subunit 1 (NFKB1) varian..:

Tuijnenburg, P ; Lango Allen, H ; Burns, SO...
https://eprints.whiterose.ac.uk/136176/7/1-s2.0-S0091674918302860-main.pdf. , 2018

Link: https://eprints.whiterose.ac.uk/136176/

RT Journal
T1 <Title>Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans</Title>

UL https://suche.suub.uni-bremen.de/peid=base-ftleedsuniv:oai:eprints.whiterose.ac.uk:136176&Exemplar=1&LAN=DE
				
A1 Tuijnenburg, P
A1 Lango Allen, H
A1 Burns, SO
A1 Greene, D
A1 Jansen, MH
A1 Staples, E
A1 Stephens, J
A1 Carss, KJ
A1 Biasci, D
A1 Baxendale, H
A1 Thomas, M
A1 Chandra, A
A1 Kiani-Alikhan, S
A1 Longhurst, HJ
A1 Seneviratne, SL
A1 Oksenhendler, E
A1 Simeoni, I
A1 de Bree, GJ
A1 Tool, ATJ
A1 van Leeuwen, EMM
A1 Ebberink, EHTM
A1 Meijer, AB
A1 Tuna, S
A1 Whitehorn, D
A1 Brown, M
A1 Turro, E
A1 Thrasher, AJ
A1 Smith, KGC
A1 Thaventhiran, JE
A1 Kuijpers, TW
A1 NIHR BioResource–Rare Diseases Consortium
PB Elsevier
YR 2018
JF https://eprints.whiterose.ac.uk/136176/7/1-s2.0-S0091674918302860-main.pdf
LK http://dx.doi.org/https://eprints.whiterose.ac.uk/136176/
DO https://eprints.whiterose.ac.uk/136176/
SF ELIB - SuUB Bremen

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