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[HTML][HTML] Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

P Tuijnenburg, HL Allen, SO Burns, D Greene… - Journal of allergy and …, 2018 - Elsevier
Background The genetic cause of primary immunodeficiency disease (PID) carries
prognostic information. Objective We conducted a whole-genome sequencing study …
被引用次数：212 相关文章

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

P Tuijnenburg, HL Allen, SO Burns… - The Journal of …, 2018 - pubmed.ncbi.nlm.nih.gov
Background The genetic cause of primary immunodeficiency disease (PID) carries
prognostic information. Objective We conducted a whole-genome sequencing study …

Loss of function NFKB1 variants are the most common monogenic cause of CVID in Europeans

P Tuijnenburg, H Lango Allen, SO Burns… - Journal of Allergy …, 2018 - discovery.ucl.ac.uk
BACKGROUND: The genetic etiology of primary immunodeficiency disease (PID) carries
prognostic information. OBJECTIVE: We conducted a whole-genome sequencing study …

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

NIHR BioResource–Rare … - … of allergy and …, 2018 - researchinformation.amsterdamumc …
Background: The genetic cause of primary immunodeficiency disease (PID) carries
prognostic information. Objective: We conducted a whole-genome sequencing study …

Loss of function NFKB1 variants are the most common monogenic cause of CVID in Europeans.

P Tuijnenburg, H Lango Allen, SO Burns, D Greene… - 2018 - repository.cam.ac.uk
BACKGROUND: The genetic etiology of primary immunodeficiency disease (PID) carries
prognostic information. OBJECTIVE: We conducted a whole-genome sequencing study …

[引用][C] Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

P Tuijnenburg, HL Allen, SO Burns, D Greene… - Journal of Allergy and …, 2018 - cir.nii.ac.jp
Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common
monogenic cause of common variable immunodeficiency in Europeans | CiNii Research …

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.

P Tuijnenburg, SO Burns, D Greene… - The Journal of Allergy …, 2018 - europepmc.org
Objective We conducted a whole-genome sequencing study assessing a large proportion of
the NIHR BioResource-Rare Diseases cohort. Methods In the predominantly European …
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[HTML][HTML] Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

P Tuijnenburg, HL Allen, SO Burns… - Journal of Allergy and …, 2018 - jacionline.org
Background The genetic cause of primary immunodeficiency disease (PID) carries
prognostic information. Objective We conducted a whole-genome sequencing study …

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans

P Tuijnenburg, H Lango Allen… - Journal of Allergy …, 2018 - eprints.whiterose.ac.uk
Background: The genetic cause of primary immunodeficiency disease (PID) carries
prognostic information. Objective: We conducted a whole-genome sequencing study …

Loss-of-function nuclear factor κB subunit 1 (NFKB1) variants are the most common monogenic cause of common variable immunodeficiency in Europeans.

P Tuijnenburg, H Lango Allen… - The Journal of …, 2018 - profiles.citeready.com
The genetic cause of primary immunodeficiency disease (PID) carries prognostic
information. We conducted a whole-genome sequencing study assessing a large proportion …