Open AccessStudying the Association between Sudden Hearing Loss and DNA N-Methyltransferase 1 (DNMT1) Genetic Polymorphism
Author(s) -
Kübra Şeker Yıldız,
Kasım Durmuş,
Gonca Dönmez,
Serdal Arslan,
Emine Elif Altuntaş
Publication year - 2017
Publication title -
the journal of international advanced otology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.518
H-Index - 13
eISSN - 2148-3817
pISSN - 1308-7649
DOI - 10.5152/iao.2017.2723
Subject(s) - genotype , medicine , haplotype , single nucleotide polymorphism , genotyping , gastroenterology , snp , polymorphism (computer science) , genetics , biology , gene
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.
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