The Analysis of GJB2, GJB3, and GJB6 Gene Mutations in Patients with Hereditary Non-Syndromic Hearing Loss Living in Sivas

OBJECTIVES: The aim of the present study was to investigate the presence of GJB2, GJB3, and GJB6 gene mutations in non-syndromic sensorineural hearing loss (NSHL) cases living in Sivas region, to provide appropriate genetic counseling for cases who were found to have mutation, and to contribute to d...

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Bibliographic Details
Published in:J Int Adv Otol
Main Authors: Kurtulgan, Hande Küçük, Altuntaş, Emine Elif, Yıldırım, Malik Ejder, Özdemir, Öztürk, Bağcı, Binnur, Sezgin, İlhan
Format: Artigo
Language:Inglês
Published: The European Academy of Otology and Neurotology 2019
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Original Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC6937194/
https://ncbi.nlm.nih.gov/pubmed/31846914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5152/iao.2019.5401
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