The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions-Reference-Cited by-同舟云学术

The spectrum of GJB2 gene mutations in Algerian families with nonsyndromic hearing loss from Sahara and Kabylie regions

Published:2019-09 Issue: Volume:124 Page:157-160
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Talbi Sonia^ORCID,Bonnet Crystel,Boudjenah Farid^ORCID,Mansouri Mohammed Tahar,Petit Christine,Ammar Khodja Fatima

Funder

Ministère de l'Enseignement Supérieur et de la Recherche Scientifique

Publisher

Elsevier BV

Subject

Otorhinolaryngology,General Medicine,Pediatrics, Perinatology, and Child Health

Reference29 articles.

1. Newborn hearing screening—a silent revolution;Morton;N. Engl. J. Med.,2006

2. DFNB1 non-syndromic hearing impairment: diversity of mutations and associated phenotypes;del Castillo;Front. Mol. Neurosci.,2017

3. Clinical features of the prevalent form of childhood deafness, DFNB1, due to a connexin-26 gene defect: implications for genetic counselling;Denoyelle;The Lancet,1999

4. Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature;Tsukada;Ann. Otol. Rhinol. Laryngol.,2015

5. Frequency of GJB2 mutations in patients with nonsyndromic hearing loss from an ethnically characterized Brazilian population;Felix;Braz. J. Otorhinolaryngol.,2017

Cited by 7 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Unraveling the Diversity of <i>GJB2</i> Mutations in Nonsyndromic Hearing Loss: A Comprehensive Study in the Moroccan Population;Audiology and Neurotology;2024

2. Research Article Mutation analysis of the GJB2 gene of patients with non-syndromic hearing impairment in the Kurdish population in Sulaimani province, Iraq;Genetics and Molecular Research;2023

3. Genetics and meta-analysis of recessive non-syndromic hearing impairment and Usher syndrome in Maghreb population: lessons from the past, contemporary actualities and future challenges;Human Genetics;2021-07-15

4. The frequency of the homozygote 35delG mutation in the connexin 26 gene in North African with non-syndromic hearing loss: A meta-analysis study;Meta Gene;2021-06

5. Screening for mitochondrial 12S rRNA C1494T mutation in 655 patients with non-syndromic hearing loss;Medicine;2020-03