Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran

Published:2014-04 Issue:4 Volume:78 Page:637-640
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Bonyadi Mortaza. J.,Fotouhi Nikou,Esmaeili Mohsen

Funder

Center of Excellence for Biodiversity (University of Tabriz)

Publisher

Elsevier BV

Subject

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

Reference25 articles.

1. Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss;Diaz-Horta;PLOS One,2012

2. Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East;Shahin;Hum. Genet.,2002

3. Cx26 deafness: mutation analysis and clinical variability;Murgia;J. Med. Genet.,1999

4. Performance of speech perception after cochlear implantation in DFNB1 patients;Dalamon;Acta Otolaryngol.,2009

5. Genetic epidemiology of hearing impairment;Morton;Ann. N. Y. Acad. Sci.,1991

Cited by 15 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. A novel method for detecting nine hotspot mutations of deafness genes in one tube;Scientific Reports;2024-01-03

2. Disease-associated variants of Gap Junction Beta 2 protein (GJB2) in the deaf population of Southern Punjab of Pakistan;PLOS ONE;2021-10-25

3. GJB2 mutations in Iranian Azeri population with autosomal recessive nonsyndromic hearing loss (ARNSHL): First report of c.238 C>A mutation in Iran;Journal of Clinical Laboratory Analysis;2021-09-28

4. Genetics of Hearing Impairment in North-Eastern Romania—A Cost-Effective Improved Diagnosis and Literature Review;Genes;2020-12-15

5. Hearing Impairment Overview in Africa: the Case of Cameroon;Genes;2020-02-22

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