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Behçet’s disease risk association fine-mapped on the IL23R–IL12RB2 intergenic region in Koreans
BACKGROUND: Behçet’s disease (BD) susceptibility had been associated with single-nucleotide polymorphisms (SNPs) in IL23R–IL12RB2, IL10, STAT4, or ERAP1 locus in Japanese, Turkish, Chinese, and other populations, but not in a Korean genome-wide association study (GWAS). We aimed to fine-map BD risk...
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| Publicado no: | Arthritis Res Ther |
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| Main Authors: | , , , , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5633897/ https://ncbi.nlm.nih.gov/pubmed/29017598 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13075-017-1435-5 |
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