The Genetic Deafness in Chinese Population
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference98 articles.
1. Prevalent connexin 26 gene(GJB2) mutations in Japanese;Abe;J Med Genet,2000
2. Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F;Ahmed;Am J Hum Genet,2001
3. The molecular genetics of Usher syndrome;Ahmed;Clin Genet,2003
4. Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F;Alagramam;Hum Mol Genet,2001
5. A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene;Bitner-Glindzicz;Nat Genet,2000
Cited by 4 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 recessive mutation in OXR1 is identified in patient with hearing loss recapitulated by the knockdown zebrafish;Human Molecular Genetics;2022-09-20
2. Chinese Sign Language Recognition with Batch Sampling ResNet-Bi-LSTM;SN Computer Science;2022-08-03
3. Assessment of Hearing Screening Combined With Limited and Expanded Genetic Screening for Newborns in Nantong, China;JAMA Network Open;2021-09-17
4. Digenic inheritance of non-syndromic deafness caused by mutations at the gap junction proteins Cx26 and Cx31;Human Genetics;2008-12-03
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