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Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss

dc.contributor.authorMumbuc, Semih
dc.contributor.authorPehlivan, Sacide
dc.contributor.authorOĞUZKAN BALCI, SİBEL
dc.contributor.authorTunc, Nihal Gungor
dc.contributor.authorKANLIKAMA, MUZAFFER
dc.contributor.authorTunc, Orhan
dc.contributor.authorBaysal, Elif
dc.date.accessioned2021-03-04T12:18:38Z
dc.date.available2021-03-04T12:18:38Z
dc.date.issued2017
dc.identifier.citationTunc O., Baysal E., OĞUZKAN BALCI S., Mumbuc S., Tunc N. G. , Pehlivan S., KANLIKAMA M., "Glutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss", ENT UPDATES, cilt.7, sa.3, ss.126-130, 2017
dc.identifier.othervv_1032021
dc.identifier.otherav_76ad736b-9210-401f-9c9d-69522d2ac4ef
dc.identifier.urihttp://hdl.handle.net/20.500.12627/81482
dc.identifier.urihttps://doi.org/10.2399/jmu.2017003003
dc.description.abstractObjective: The aim of this study was to search the codon 200 polymorphism on the glutathione peroxidase 1 gene (GPX1) and A/T changes on the promoter region of the catalase gene (CAT) in cochlear implant patients with congenital profound hearing loss.
dc.language.isoeng
dc.subjectTıp
dc.subjectKulak Burun Boğaz
dc.subjectSağlık Bilimleri
dc.subjectKlinik Tıp (MED)
dc.subjectKlinik Tıp
dc.subjectKULAK BURUN BOĞAZ
dc.subjectCerrahi Tıp Bilimleri
dc.titleGlutathione peroxidase and catalase enzyme gene polymorphisms in profound congenital hearing loss
dc.typeMakale
dc.relation.journalENT UPDATES
dc.contributor.departmentCengiz Gokcek Hosp , ,
dc.identifier.volume7
dc.identifier.issue3
dc.identifier.startpage126
dc.identifier.endpage130
dc.contributor.firstauthorID247923


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