Article

Relevance of Connexin 26 (GJB2) Gene Mutations With Congenital Nonsyndromic Sensorineural Hearing Loss in Lraqi Deafness Patients.

2021-01-15

Abstract excerpt

<title>Abstract</title> <p><bold>Objective: </bold>This study aimed to detect the frequency of the three most common mutations of GJB2 in nonsyndromic sensorineural deafness for Iraqi population.<bold>Method: </bold>The current case-control study was conducted from January 2018 to November 2019 at ENT Departments from middle Euphrates region of Iraq. The study was included 95 deaf patients group (55 males and 40...

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Literature Corpus work: aea01fae-90df-56cb-8df9-af729b8c9327
DOI: 10.21203/rs.3.rs-139090/v1

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