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Author = Maryam Hajilari
Number of Articles: 2
Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran
Volume 11, Issue 1 , January 2023, , Pages 17286-17298
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 MoreHereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study
Volume 7, Issue 11 , November 2019, , Pages 10323-10334