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Article

KIR3DL1/S1 Allotypes Contribute Differentially to the Development of Behçet Disease.

Journal of immunology (Baltimore, Md. : 1950) - 15 Sept 2019

Petrushkin Harry, Norman Paul J, Lougee Emma, Parham Peter, Wallace Graham R, Stanford Miles R, Fortune Farida

Abstract excerpt

Behçet disease is a chronic, relapsing-remitting autoinflammatory syndrome with a strong HLA-B*51 association. In this paper, we describe a human cohort of 267 individuals with Behçet disease and 445 matched controls from a tertiary referral center in the U.K. HLA-B*51 was confirmed as a genetic risk factor in this group (p = 0.0006, Bonferroni-Dunn correction for multiple testing [Pc] = 0.0192, odds ratio [OR]...

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Source

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Identifiers

PMID: 31405953
DOI: 10.4049/jimmunol.1801178
PMCID: PMC6731450

Genes

KIR3DL1
KIR3DS1

Provenance

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

Source receipt: pubmed, retrieved 7 Sept 2026.

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