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Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF

dc.contributor.authorUgurlu, S.
dc.contributor.authorOzdogan, H.
dc.contributor.authorTolun, A.
dc.contributor.authorTuranli, E. Tahir
dc.contributor.authorKaracan, I.
dc.date.accessioned2021-03-03T11:44:09Z
dc.date.available2021-03-03T11:44:09Z
dc.date.issued2017
dc.identifier.citationKaracan I., Ugurlu S., Tolun A., Turanli E. T. , Ozdogan H., "Other autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF", CLINICAL AND EXPERIMENTAL RHEUMATOLOGY, cilt.35, sa.6, 2017
dc.identifier.issn0392-856X
dc.identifier.othervv_1032021
dc.identifier.otherav_29a10a81-9943-4b71-8a86-794942d97d4b
dc.identifier.urihttp://hdl.handle.net/20.500.12627/32798
dc.description.abstractObjective. No MEFV mutations are detected in approximately 10% of the patients with clinical FMF in populations where the disease is highly prevalent. Causative mutations were searched in other genes in two such families with "MEFV negative clinical FMF".
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.titleOther autoinflammatory disease genes in an FMF-prevalent population: a homozygous MVK mutation and a heterozygous TNFRSF1A mutation in two different Turkish families with clinical FMF
dc.typeMakale
dc.relation.journalCLINICAL AND EXPERIMENTAL RHEUMATOLOGY
dc.contributor.departmentİstanbul Üniversitesi , ,
dc.identifier.volume35
dc.identifier.issue6
dc.contributor.firstauthorID239389


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