Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran

Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran

Background: Hereditary Hearing Loss (HL) is one of the most prevalent sensorineural disorders worldwide. Several hundreds of genes have been reported to have associations with this condition. Autosomal Recessive Non-Syndromic Hearing Loss (ARNSHL), with the highest frequency of severe to profound ty...

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Bibliographic Details
Main Authors: Maryam Hajilari, Atefeh Sharifinya, Teymoor Khosravi, Anvarsadat Kianmehr, Mohammad Hossein Taziki, Ayyoob Khosravi, Morteza Oladnabi
Format: Article
Language:English
Published: Mashhad University of Medical Sciences 2023-01-01
Series:International Journal of Pediatrics
Subjects:
hearing loss,,
,،c.35delg mutation,,
,،gjb2 gene,,
,،connexin 26,,
,،autosomal recessive nonsyndromic hearing loss (arnshl)
Online Access:https://ijp.mums.ac.ir/article_21658_d458432d44767aa8334eceb5c6a86f56.pdf

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https://ijp.mums.ac.ir/article_21658_d458432d44767aa8334eceb5c6a86f56.pdf

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