RT Journal Article
SR Electronic
A1 Buckley, Rita
T1 Genome-Wide Analysis of Imputed Genotypes Identifies CCR1/CCR3 as Novel Risk Locus in Behçet Disease
JF MD Conference Express
YR 2011
FD SAGE Publications
VO 11
IS 13
SP 17
OP 18
DO 10.1177/155989771113011
UL http://mdc.sagepub.com/content/11/13/17.2.abstract
AB Behçet disease (BD) is a genetically complex condition that is characterized by recurrent inflammatory attacks that affect the orogenital mucosa, eyes, and skin. Genomewide association studies have linked the IL10 and IL23R-IL12RB2 loci to BD susceptibility [Remmers EF et al. Nat Genet 2010; Mizuki N et al. Nat Genet 2010].