Volume 12 (2024)
Volume 11 (2023)
Volume 10 (2022)
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Volume 1 (2013)
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

Maryam Hajilari; Atefeh Sharifinya; Teymoor Khosravi; Anvarsadat Kianmehr; Mohammad Hossein Taziki; Ayyoob Khosravi; Morteza Oladnabi

Volume 11, Issue 1 , January 2023, , Pages 17286-17298

https://doi.org/10.22038/ijp.2023.69158.5122

Abstract
  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 ...  Read More