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