Maternally Inherited Aminoglycoside-Induced and Nonsyndromic Deafness Is Associated with the Novel C1494T Mutation in the Mitochondrial 12S rRNA Gene in a Large Chinese Family
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference49 articles.
1. Sequence and organization of the human mitochondrial genome;Anderson;Nature,1981
2. Gapped BLAST and PSI-BLAST: a new generation of protein database search programs;Altschul;Nucleic Acids Res,1997
3. Susceptibility mutations in the mitochondrial small ribosomal RNA gene in aminoglycoside induced deafness;Bacino;Pharmacogenetics,1995
4. The mtDNA-encoded ND6 subunit of mitochondrial NADH dehydrogenase is essential for the assembly of the membrane arm and the respiratory function of the enzyme;Bai;EMBO J,1998
5. Sequence and gene organization of mouse mitochondrial DNA;Bibb;Cell,1981
Cited by 296 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. Col1a1 mediates the focal adhesion pathway affecting hearing in miR-29a mouse model by RNA-seq analysis;Experimental Gerontology;2024-01
2. Aminoglycosides-Related Ototoxicity: Mechanisms, Risk Factors, and Prevention in Pediatric Patients;Pharmaceuticals;2023-09-25
3. Induced pluripotent stem cells: ex vivo models for human diseases due to mitochondrial DNA mutations;Journal of Biomedical Science;2023-09-22
4. Maternally inherited non-syndromic hearing loss is linked with a novel mitochondrial ND6 gene mutation;Irish Journal of Medical Science (1971 -);2023-08-10
5. Gene Screening for Non-Syndromic Deafness in Hainanese Patients;The Journal of International Advanced Otology;2023-08-01
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