Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Two novel compound heterozygous families with a trimutation in the GJB2 gene causing sensorineural hearing loss

Published:2015-12 Issue:12 Volume:79 Page:2295-2299
ISSN:0165-5876
Container-title:International Journal of Pediatric Otorhinolaryngology
language:en
Short-container-title:International Journal of Pediatric Otorhinolaryngology

Author:

Martínez-Saucedo M.,Rivera-Vega M.R.,Gonzalez-Huerta L.,Urueta-Cuellar H.,Toral-López J.,Berruecos-Villalobos P.,Cuevas-Covarrubias S.

Funder

DGAPA PAPIIT

Publisher

Elsevier BV

Subject

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

Reference18 articles.

1. Possible interaction between USH1B and USH3 gene products as implied by apparent digenic deafness inheritance;Adato;Am. J. Hum. Genet.,1999

2. A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: a novel founder mutation in Ashkenazi Jews;Lerer;Hum. Mutat.,2001

3. Mutation in the mitochondrial 12S rRNA gene in two families from Mongolia with matrilineal aminoglycoside ototoxicity;Pandya;J. Med. Genet.,1997

4. Dominant modifier DFNM1 suppresses recessive deafness DFNB26;Riazuddin;Nat. Genet.,2000

5. ENU mutagenesis and the search for deafness genes;Hardisty;Br. J. Audiol.,1999

Cited by 6 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. First report of an Ivorian family with nonsyndromic hearing loss caused by GJB2 compound heterozygous variants;Annals of Human Genetics;2024-08-02

2. Congenital hearing loss: a literature review of the genetic etiology in a Mexican population;Boletín Médico del Hospital Infantil de México;2022-09-14

3. Genetic etiology of non-syndromic hearing loss in Latin America;Human Genetics;2021-10-15

4. Systematic Review of Pathogenic GJB2 Variants in the Latino Population;Otology & Neurotology;2020-02

5. GJB2 and GJB6 Mutations in Non-Syndromic Childhood Hearing Impairment in Ghana;Frontiers in Genetics;2019-09-18

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