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Article

[De novo NFκB2 gene mutation associated common variable immunodeficiency].

Zhonghua er ke za zhi = Chinese journal of pediatrics - 2 Aug 2018

Luo M Z, Xu T, Xue X H, Wang Y P, Wu P L, Chen X M, Tang X M, Zhao X D, Zhang Z Y

Abstract excerpt

Objective: To investigate the clinical, immunological, and molecular manifestations of nuclear factor kappa-B subunit 2 (NFκB2) gene mutation associated common variable immunodeficiency (CVID) . Methods: A 14-month-old boy diagnosed with NFκB2-mutated CVID was admitted into Children's Hospital of Chongqing Medical University in December 2015. The clinical manifestations, biochemical tests, immunological function,...

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PMID: 30078247
DOI: 10.3760/cma.j.issn.0578-1310.2018.08.014

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

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