Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Etiology and associated GJB2 mutations in Mauritanian children with non-syndromic hearing loss

Published:2016-04-11 Issue:11 Volume:273 Page:3693-3698
ISSN:0937-4477
Container-title:European Archives of Oto-Rhino-Laryngology
language:en
Short-container-title:Eur Arch Otorhinolaryngol

Author:

Moctar Ely Cheikh Mohamed,Riahi Zied,El Hachmi Hala,Veten Fatimetou,Meiloud Ghlana,Bonnet Christine,Abdelhak Sonia,Errami Mohammed,Houmeida Ahmed

Publisher

Springer Science and Business Media LLC

Subject

General Medicine,Otorhinolaryngology

Link

http://link.springer.com/content/pdf/10.1007/s00405-016-4036-z.pdf

Reference39 articles.

1. Fact sheet No. 300 on deafness and hearing loss [WHO Web site]. http://www.who.int/mediacentre/factsheets/fs300/en/ . Accessed May 13 2015

2. Morton CC, Nance WE (2006) Newborn hearing screening—a silent revolution. Engl J Med 18:2151–2164

3. Javidnia H, Carson N, Awubwa M, Byaruhanga R, Mack D, Vaccani JP (2014) Connexin gene mutations among Ugandan patients with nonsyndromic sensorineural hearing loss. Laryngoscope 124:373–376

4. Chan DK, Chang KW (2014) GJB2-associated hearing loss: systematic review of worldwide prevalence, genotype, and auditory phenotype. Laryngoscope 124:34–53

5. Zelante L, Gasparini P, Estivill X, Melchionda S, D’Agruma L, Govea N et al (1997) Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans. Hum Mol Genet 6:1605–1609

Cited by 16 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. Splice-altering variant of PJVK gene in a Mauritanian family with non-syndromic hearing impairment;Journal of Applied Genetics;2024-09-04

2. First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants;Annals of Human Genetics;2024-08-02

3. The genetic basis and the diagnostic yield of genetic testing related to nonsyndromic hearing loss in Qatar;Scientific Reports;2024-02-20

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

5. Identification a novel pathogenic LRTOMT mutation in Mauritanian families with nonsyndromic deafness;European Archives of Oto-Rhino-Laryngology;2023-03-16

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线，采集、加工和组织学术论文而形成的新型学术文献查询和分析系统，可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容，当前同舟云学术共收录了国内外主流学术期刊6万余种，收集的期刊论文及会议论文总量共计约1.5亿篇，并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询！咨询电话：010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号京ICP备18003416号-3