Article

Connexin 26 (GJB2) Gene Mutations Linked With Autosomal Recessive Nonsyndromic Sensorineural Hearing Loss in Iraqi Population.

2021-05-25

Abstract excerpt

<title>Abstract</title> <p>Objectives<bold>: </bold>The ARNSHL wasn’t been studied enough in Iraq, this study aimed to detect the prevalence of the three most common mutations of Connexin 26 gene in Iraqi population.<bold> </bold>This study was conducted in order to detect c.35delG, c.235delC and c.167delT mutations in GJB2 gene, we were employed PCR-RFLP assays. <h4>Results:</h4> The current case-control study w...

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Literature Corpus work: 953d6b16-08d9-5bee-9c67-bdb813643f4e
DOI: 10.21203/rs.3.rs-270492/v2

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