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Characterization of the clinical and immunologic phenotype and management of 157 individuals with 56 distinct heterozygous NFKB1 mutations. (2020)

First Author: Lorenzini T

Attributed to: ISCF HDRUK DIH Sprint Exemplar: Cloud-based integration of phenotype and genotype data for rare disease research funded by ISCF

Abstract

No abstract provided

Bibliographic Information

Digital Object Identifier: http://dx.doi.org/10.1016/j.jaci.2019.11.051

PubMed Identifier: 32278790

Publication URI: http://europepmc.org/abstract/MED/32278790

Type: Journal Article/Review

Volume: 146

Parent Publication: The Journal of allergy and clinical immunology

Issue: 4

ISSN: 0091-6749