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Whole-genome screening for susceptibility genes in multicase families with Behcet's disease

dc.contributor.authorOLLIER, WE
dc.contributor.authorGul, Ahmet
dc.contributor.authorSILMAN, AJ
dc.contributor.authorWORTHINGTON, J
dc.contributor.authorKARASNEH, J
dc.date.accessioned2021-03-04T08:58:49Z
dc.date.available2021-03-04T08:58:49Z
dc.date.issued2005
dc.identifier.citationKARASNEH J., Gul A., OLLIER W., SILMAN A., WORTHINGTON J., "Whole-genome screening for susceptibility genes in multicase families with Behcet's disease", ARTHRITIS AND RHEUMATISM, cilt.52, sa.6, ss.1836-1842, 2005
dc.identifier.issn0004-3591
dc.identifier.otherav_660d53b3-b32f-4018-8efd-cff35d579160
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/70887
dc.identifier.urihttps://doi.org/10.1002/art.21060
dc.description.abstractObjective. Behcet's disease is generally considered to be a multifactorial disease with important genetic and environmental components. A strong association between an HLA class I antigen, HLA-B51, and Behcet's disease has long been known. However, analysis of multicase families has suggested a substantial contribution of non-HLA loci. The aim of this study was to perform a whole-genome linkage analysis for identification of other susceptibility loci for Behcet's disease in multicase families.
dc.language.isoeng
dc.subjectSağlık Bilimleri
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleWhole-genome screening for susceptibility genes in multicase families with Behcet's disease
dc.typeMakale
dc.relation.journalARTHRITIS AND RHEUMATISM
dc.contributor.department, ,
dc.identifier.volume52
dc.identifier.issue6
dc.identifier.startpage1836
dc.identifier.endpage1842
dc.contributor.firstauthorID50840


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