"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

"Frequency of A Very Rare 35delG Mutation in Two Ethnic Groups of Iranian Populations "

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The 35delG mutation in the Connexin 26 gene (Cx26), at the DNFB1 locus is the most common mutation in the patients with autosomal recessive non-syndromic hearing loss (ARNSHL). We have studied a total of 224 deaf cases from 189 families in two populations of Iran (Sistan va Bluchestan and Hormozgan...

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Bibliographic Details
Main Authors: R Sasanfar, A Tolouei, A Hoseinipour, DD Farhud, M Dolati, L Hoghooghi Rad, M Montazer Zohour, M Ghadami, H Pour-Jafari, M Hashemzadeh Chaleshtori
Format: Article
Language:English
Published: Tehran University of Medical Sciences 2004-12-01
Series:Iranian Journal of Public Health
Subjects:
Mutation
Autosomal recessive non-syndromic hearing loss
Online Access:https://ijph.tums.ac.ir/index.php/ijph/article/view/1888

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