GJB2 ‐related hearing loss in central Iran: Review of the spectrum and frequency of gene mutations
Author:
Affiliation:
1. Cancer Research Center Shahrekord University of Medical Sciences Shahrekord Iran
2. Department of Medical Physics, School of Medicine Isfahan University of Medical Sciences Isfahan Iran
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/ahg.12354
Reference58 articles.
1. Prevalent connexin 26 gene (GJB2) mutations in Japanese
2. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India
3. Spectrum of GJB2 Mutations in a Cohort of Nonsyndromic Hearing Loss Cases from the Kingdom of Saudi Arabia
4. Mutations in GJB2 as Major Causes of Autosomal Recessive Non-Syndromic Hearing Loss: First Report of c.299-300delAT Mutation in Kurdish Population of Iran
5. Update of spectrum c.35delG and c.‐23+1G>A mutations on the GJB2 gene in individuals with autosomal recessive nonsyndromic hearing loss
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4. Frequency of c.35delG Mutation in GJB2 gene in Patients with Autosomal Recessive Non-Syndromic Hearing Loss of Five Ethnic Groups in Golestan, Iran;INT J PEDIATR-MASSHA;2023
5. Non-Syndromic Hearing Loss in a Romanian Population: Carrier Status and Frequent Variants in the GJB2 Gene;Genes;2022-12-26
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