Mutation Identification in Exon 10 of SLC26A4 Gene in Individuals with Hearing Loss in Guilan Province
Introduction: Mutation in SLC26A4 gene is one of reason of syndromic and non-syndomic hearing loss. Mutation in this gene is reported to be the second most common cause of deafness in the worldwide, after GJB2 gene. The aim of this study was to evaluate mutations in exon 10 of SLC26A4 gene in indivi...
Main Authors: | , , |
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Format: | Article |
Language: | fas |
Published: |
Alborz University of Medical Sciencs
2020-04-01
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Series: | Bihdād |
Subjects: | |
Online Access: | http://aums.abzums.ac.ir/article-1-1081-en.html |