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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations

Research output: Contribution to journal › Article › Academic › peer-review

DOI

https://doi.org/10.1016/j.jaci.2019.11.051
Final published version

NIHR-BioResource – Rare Diseases Consortium

Original language	English
Pages (from-to)	901-911
Number of pages	11
Journal	Journal of allergy and clinical immunology
Volume	146
Issue number	4
Early online date	2020
DOIs	https://doi.org/10.1016/j.jaci.2019.11.051
Publication status	Published - Oct 2020

Research areas

NF-κB1-related phenotype, NFKB1 mutation, NFKB1 variant, autosomal dominant, common variable immunodeficiency, reduced penetrance

ID: 11679137