PT  - JOURNAL ARTICLE
AU  - Buckley, Rita
ED  - Kirino, Yohei
TI  - Genome-Wide Analysis of Imputed Genotypes Identifies CCR1/CCR3 as Novel Risk Locus in Behçet Disease
DP  - 2011  01
TA  - MD Conference Express
PG  - 17--18
VI  - 11
IP  - 13
4099  - http://mdc.sagepub.com/content/11/13/17.2.short
4100  - http://mdc.sagepub.com/content/11/13/17.2.full
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].