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dc.contributor.authorCakiris, Aris
dc.contributor.authorHATEMI, Gülen
dc.contributor.authorGuel, A.
dc.contributor.authorCosan, F.
dc.contributor.authorKasapcopur, Oe.
dc.contributor.authorUestek, D.
dc.contributor.authorEkmekci, C.
dc.contributor.authorOku, B.
dc.contributor.authorAbaci, N.
dc.contributor.authorCELIK, S.
dc.contributor.authorKamali, S.
dc.contributor.authorOEZDOGAN, H.
dc.date.accessioned2021-03-06T12:52:16Z
dc.date.available2021-03-06T12:52:16Z
dc.date.issued2008
dc.identifier.citationUestek D., Ekmekci C., Oku B., Cosan F., Cakiris A., Abaci N., CELIK S., Kamali S., HATEMI G., Kasapcopur O., et al., "MEFV gene 3'-UTR Alu repeat polymorphisms in patients with familial Mediterranean fever", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.26, 2008
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_f5f5cf97-b563-4f95-b9e5-5357e8e16f0c
dc.identifier.urihttp://hdl.handle.net/20.500.12627/161167
dc.description.abstractObjective. Familial Mediterranean fever (FMF), an autosomal recessively inherited outoinflammatory disorder, is caused by missense mutations in the pyrin-encoding MEFV gene. The MEFV initiations can be detected in the majority of FMF patients. but there is an important proportion of patients with the FMF phenotype who carry a single or no coding region initiation. This study aimed to investigate the promoter region and 3'-UTR polymorphisms of the MEFV gene in a group of FMF patients with no coding region mutations. to identify variations with a possible role in the regulation of MEFV expression.
dc.language.isoeng
dc.subjectİmmünoloji ve Romatoloji
dc.subjectDahili Tıp Bilimleri
dc.subjectİç Hastalıkları
dc.subjectSağlık Bilimleri
dc.subjectTıp
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectROMATOLOJİ
dc.titleMEFV gene 3'-UTR Alu repeat polymorphisms in patients with familial Mediterranean fever
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume26
dc.identifier.issue4
dc.contributor.firstauthorID218


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