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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Detalles Bibliográficos
Autores principales: Kang, Eun Ha, Kim, Sewon, Park, Min Young, Choi, Ji Yong, Choi, In Ah, Kim, Min Jung, Ha, You-Jung, Lee, Eun Young, Lee, Yun Jong, Lee, Eun Bong, Kang, Changwon, Song, Yeong Wook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633897/
https://www.ncbi.nlm.nih.gov/pubmed/29017598
http://dx.doi.org/10.1186/s13075-017-1435-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5633897/
https://www.ncbi.nlm.nih.gov/pubmed/29017598
http://dx.doi.org/10.1186/s13075-017-1435-5

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