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dc.contributor.authorOzvarnali, Ayla
dc.contributor.authorCefle, Kıvanç
dc.contributor.authorCoskunpinar, Ender
dc.contributor.authorOzturk, Derya
dc.contributor.authorPalanduz, Ayse
dc.contributor.authorGül, Ahmet
dc.contributor.authorOzturk, Sukru
dc.contributor.authorPalanduz, Sukru
dc.date.accessioned2021-03-04T19:46:16Z
dc.date.available2021-03-04T19:46:16Z
dc.date.issued2018
dc.identifier.citationCoskunpinar E., Ozvarnali A., Cefle K., Palanduz A., Gül A., Ozturk D., Ozturk S., Palanduz S., "Molecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene", HASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI, cilt.56, ss.42-49, 2018
dc.identifier.othervv_1032021
dc.identifier.otherav_915afba7-ecb6-4e8c-ae2b-413e65e4ae7f
dc.identifier.urihttp://hdl.handle.net/20.500.12627/98078
dc.identifier.urihttps://doi.org/10.4274/haseki.42714
dc.description.abstractAim: Familial Mediterranean Fever (FMF) is the most frequent and historically the oldest autosomal recessive autoinflammatory disorder. No pathogen or auto-antibody has been shown to be associated with FMF. The disorder manifests with bouts of fever and abdominal pain, which are called "attacks". In the present study, we aimed to find the most frequent mutations in the MEFV gene in the Turkish population.
dc.language.isoeng
dc.subjectTıp
dc.subjectSağlık Bilimleri
dc.subjectTemel Tıp Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectTIP, GENEL & İÇECEK
dc.titleMolecular Diagnosis Experience in Familial Mediterranean Fever: The Most Frequent Mutations in the MEFV Gene
dc.typeMakale
dc.relation.journalHASEKI TIP BULTENI-MEDICAL BULLETIN OF HASEKI
dc.contributor.departmentİstanbul Teknik Üniversitesi , Fen-Edebiyat , Kimya
dc.identifier.volume56
dc.identifier.issue1
dc.identifier.startpage42
dc.identifier.endpage49
dc.contributor.firstauthorID26846


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