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

Tunc O., Baysal E., OĞUZKAN BALCI S., Mumbuc S., Tunc N. G., Pehlivan S., ...Daha Fazla

ENT UPDATES, cilt.7, sa.3, ss.126-130, 2017 (ESCI) identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 7 Sayı: 3
  • Basım Tarihi: 2017
  • Doi Numarası: 10.2399/jmu.2017003003
  • Dergi Adı: ENT UPDATES
  • Derginin Tarandığı İndeksler: Emerging Sources Citation Index (ESCI), TR DİZİN (ULAKBİM)
  • Sayfa Sayıları: ss.126-130
  • İstanbul Üniversitesi Adresli: Evet

Özet

Objective: 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.