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Evaluation of the GJB2 and GJB6 Polymorphisms with Autosomal Recessive Nonsyndromic Hearing Loss in Iranian Population

INTRODUCTION: Hearing loss (HL), with more than 100 gene loci, is the most common sensorineural defects in humans. The mutations in two GJB2 and GJB6 (Gap Junction Protein Beta 2, 6) genes are responsible for nearly 50% of autosomal recessive nonsyndromic hearing loss. The aim of the present study w...

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Bibliografiske detaljer
Udgivet i:Iran J Otorhinolaryngol
Main Authors: Ebrahimkhani, Somayeh, Asaadi Tehrani, Golnaz
Format: Artigo
Sprog:Inglês
Udgivet: Mashhad University of Medical Sciences 2021
Fag:
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8052483/
https://ncbi.nlm.nih.gov/pubmed/33912482
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.22038/ijorl.2020.45196.2483
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