Identities, frequencies and origins ofTMC1mutations causing DFNB7/B11 deafness in Pakistan
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.2007.00895.x/fullpdf
Reference18 articles.
1. Autosomal and X-Linked Auditory Disorders
2. Human nonsyndromic sensorineural deafness;Friedman;Annu Rev Genomics Hum Genet,2003
3. Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function;Kurima;Nat Genet,2002
4. Mutation screening of TMC1 in DFNB7/11 families;Yang;Am J Hum Genet,2002
5. Beethoven, a mouse model for dominant, progressive hearing loss DFNA36;Vreugde;Nat Genet,2002
Cited by 60 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. CIB2 as a Ca2+Sensor for Auditory Mechano-Electrical Transduction and Linked to Genetic-Heterogeneity ofTMC1in Hearing Loss;2024-07-24
2. Genetic analysis of 106 sporadic cases with hearing loss in the UAE population;Human Genomics;2024-06-07
3. Autosomal recessive non‐syndromic hearing loss genes in Pakistan during the previous three decades;Journal of Cellular and Molecular Medicine;2024-03-27
4. Functional consequences of Genetics variant in TMC1 and TMC2 within a United Arab Emirates family with Pre-lingual hearing loss;Saudi Journal of Biological Sciences;2023-02
5. Biallelic mutations in pakistani families with autosomal recessive prelingual nonsyndromic hearing loss;Genes & Genomics;2022-12-06
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