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DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome

dc.contributor.authorFan, Yao-Shan
dc.contributor.authorKasapcopur, Ozgur
dc.contributor.authorDiaz-Horta, Oscar
dc.contributor.authorYalcinkaya, Fatos
dc.contributor.authorTekin, Mustafa
dc.contributor.authorOzcakar, Z. Birsin
dc.contributor.authorFoster, Joseph
dc.date.accessioned2021-03-03T11:23:36Z
dc.date.available2021-03-03T11:23:36Z
dc.date.issued2013
dc.identifier.citationOzcakar Z. B. , Foster J., Diaz-Horta O., Kasapcopur O., Fan Y., Yalcinkaya F., Tekin M., "DNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome", ARTHRITIS AND RHEUMATISM, cilt.65, sa.8, ss.2183-2189, 2013
dc.identifier.issn0004-3591
dc.identifier.otherav_27af961f-2bde-402b-8358-f7e3574a429b
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/31528
dc.identifier.urihttps://doi.org/10.1002/art.38010
dc.description.abstractObjective. Hypocomplementemic urticarial vasculitis syndrome (HUVS) is characterized by recurrent urticaria along with dermal vasculitis, arthritis, and glomerulonephritis. Systemic lupus erythematosus (SLE) develops in >50% of patients with HUVS, although the pathogenesis is unknown. The aim of this study was to identify the causative DNA mutations in 2 families with autosomal-recessive HUVS, in order to reveal the pathogenesis and facilitate the laboratory diagnosis.
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.titleDNASE1L3 Mutations in Hypocomplementemic Urticarial Vasculitis Syndrome
dc.typeMakale
dc.relation.journalARTHRITIS AND RHEUMATISM
dc.contributor.departmentAnkara Üniversitesi , ,
dc.identifier.volume65
dc.identifier.issue8
dc.identifier.startpage2183
dc.identifier.endpage2189
dc.contributor.firstauthorID42441


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