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A single endoplasmic reticulum aminopeptidase-1 protein allotype is a strong risk factor for Behcet's disease in HLA-B(star)51 carriers

dc.contributor.authorTugal-Tutkun, Ilknur
dc.contributor.authorSeyahi, Emire
dc.contributor.authorErer, Burak
dc.contributor.authorOzyazgan, Yilmaz
dc.contributor.authorGül, Ahmet
dc.contributor.authorTAKEUCHI, Masaki
dc.contributor.authorKIRINO, Yohei
dc.contributor.authorOMBRELLO, Michael J.
dc.contributor.authorWATTS, Norman R.
dc.contributor.authorKASTNER, Daniel L.
dc.contributor.authorREMMERS, Elaine F.
dc.date.accessioned2021-03-05T14:05:48Z
dc.date.available2021-03-05T14:05:48Z
dc.date.issued2016
dc.identifier.citationTAKEUCHI M., OMBRELLO M. J. , KIRINO Y., Erer B., Tugal-Tutkun I., Seyahi E., Ozyazgan Y., WATTS N. R. , Gül A., KASTNER D. L. , et al., "A single endoplasmic reticulum aminopeptidase-1 protein allotype is a strong risk factor for Behcet's disease in HLA-B(star)51 carriers", ANNALS OF THE RHEUMATIC DISEASES, cilt.75, ss.2208-2211, 2016
dc.identifier.issn0003-4967
dc.identifier.othervv_1032021
dc.identifier.otherav_b56f583c-e330-4312-8f15-1421942048b1
dc.identifier.urihttp://hdl.handle.net/20.500.12627/120806
dc.identifier.urihttps://doi.org/10.1136/annrheumdis-2015-209059
dc.description.abstractIntroduction Endoplasmic reticulum aminopeptidase-1 (ERAP1) protein is highly polymorphic with numerous missense amino acid variants. We sought to determine the naturally occurring ERAP1 protein allotypes and their contribution to Behcet's disease.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİç Hastalıkları
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleA single endoplasmic reticulum aminopeptidase-1 protein allotype is a strong risk factor for Behcet's disease in HLA-B(star)51 carriers
dc.typeMakale
dc.relation.journalANNALS OF THE RHEUMATIC DISEASES
dc.contributor.departmentNational Institutes of Health (NIH) - USA , ,
dc.identifier.volume75
dc.identifier.issue12
dc.identifier.startpage2208
dc.identifier.endpage2211
dc.contributor.firstauthorID51308


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