Non-Syndromic Hearing Loss and High-Throughput Strategies to Decipher Its Genetic Heterogeneity
Author:
Publisher
Elsevier BV
Subject
Otorhinolaryngology
Reference157 articles.
1. Mutations of MYO6 are associated with recessive deafness, DFNB37;Ahmed;Am. J. Hum. Genet.,2003
2. PCDH15 is expressed in the neurosensory epithelium of the eye and ear and mutant alleles are responsible for both USH1F and DFNB23;Ahmed;Hum. Molec. Genet.,2003
3. SLC26A4 gene is frequently involved in nonsyndromic hearing impairment with enlarged vestibular aqueduct in Caucasian populations;Albert;European Journal of Human Genetics,2006
4. The genetic bases for syndromic and nonsyndromic deafness among Jews;Ben-Yosef;Trends Mol Med,2001
5. Hereditary deafness and phenotyping in humans;Bitner-Glindzicz;Br Med Bull.,2002
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. Advanced Omics Techniques for Understanding Cochlear Genome, Epigenome, and Transcriptome in Health and Disease;Biomolecules;2023-10-17
2. Epidemiology, etiology, genetic variants in non- syndromic hearing loss in Iran: A systematic review and meta‐analysis;International Journal of Pediatric Otorhinolaryngology;2023-05
3. Functional Annotation and Analysis of Genetic Variants;IEEE Access;2023
4. Identification of GJB2 Variants in 75 Unrelated Iranian Autosomal Recessive Non-syndromic Hearing Loss Patients;Journal of Human Genetics and Genomics;2022-02-22
5. Visualization of Functional Assignment of Disease Genes and Mutations;Communications in Computer and Information Science;2022
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