Pathogenic mitochondrial DNA mutations in protein-coding genes
Author:
Publisher
Wiley
Subject
Physiology (medical),Cellular and Molecular Neuroscience,Neurology (clinical),Physiology
Reference117 articles.
1. Mitochondrial T9957C Mutation in Association with NAION and Seizures but not MELAS
2. Mitochondrial Abnormalities in Patients with LHON-like Optic Neuropathies
3. Missense mutation in the mtDNA cytochrome b gene in a patient with myopathy
4. A nonsense mutation (G15059A) in the cytochromeb gene in a patient with exercise intolerance and myoglobinuria
5. Polymorphic Variants in the Human Mitochondrial CytochromebGene
Cited by 103 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. The Dawn and Advancement of the Knowledge of the Genetics of Migraine;Journal of Clinical Medicine;2024-05-04
2. Elderly onset of MELAS carried an M.3243A >G mutation in a female with deafness and visual deficits: A case report;Clinical Case Reports;2024-03
3. Stroke-Like Episodes in Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS);Stroke Genetics;2024
4. Inborn Errors of Carbohydrate, Ammonia, Amino Acid, and Organic Acid Metabolism;Avery's Diseases of the Newborn;2024
5. Efficient elimination of MELAS-associated m.3243G mutant mitochondrial DNA by an engineered mitoARCUS nuclease;Nature Metabolism;2023-11-30
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