Mutation Identification in Exon 10 of SLC26A4 Gene in Individuals with Hearing Loss in Guilan Province

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...

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Bibliographic Details
Main Authors: Omid Rezaei, Najmeh Ranji, Zeinab Khazaei Koohpar
Format: Article
Language:fas
Published: Alborz University of Medical Sciencs 2020-04-01
Series:Bihdād
Subjects:
hearing loss
exon 10
mutation
slc26a4 gene
Online Access:http://aums.abzums.ac.ir/article-1-1081-en.html

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