Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism

Yildiz, Kubra; DURMUŞ, KASIM; DÖNMEZ, GONCA; ARSLAN, SERDAL; ALTUNTAŞ, EMİNE

doi:10.5152/iao.2017.2723

Studying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism

Yildiz K. S., DURMUŞ K., DÖNMEZ G., ARSLAN S., ALTUNTAŞ E. E.

JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY, cilt.13, sa.3, ss.313-317, 2017 (SCI-Expanded, Scopus)

Yayın Türü: Makale / Tam Makale
Cilt numarası: 13 Sayı: 3
Basım Tarihi: 2017
Doi Numarası: 10.5152/iao.2017.2723
Dergi Adı: JOURNAL OF INTERNATIONAL ADVANCED OTOLOGY
Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
Sayfa Sayıları: ss.313-317
Açık Arşiv Koleksiyonu: AVESİS Açık Erişim Koleksiyonu
Sivas Cumhuriyet Üniversitesi Adresli: Evet

Özet

OBJECTIVE: The aim of the present study was to investigate whether there was any relationship between some DNA N-methyltransferase 1 (DNMT1) polymorphisms and susceptibility to idiopathic sudden sensorineural hearing loss (ISSHL) in ISSHL patients.