Leber hereditary optic neuropathy due to a new ND1 mutation-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Leber hereditary optic neuropathy due to a new ND1 mutation

Published:2017-01-31 Issue:5 Volume:38 Page:480-485
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Soldath Patrick¹²,Wegener Marianne¹³,Sander Birgit³,Rosenberg Thomas¹³,Duno Morten⁴,Wibrand Flemming⁴,Vissing John¹²

Affiliation:

1. Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

2. Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen, Denmark

3. Department of Ophthalmology, Rigshospitalet, Copenhagen, Denmark

4. Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2016.1253108

Reference33 articles.

1. Mitochondrial dysfunction as a cause of optic neuropathies

2. Inherited mitochondrial optic neuropathies

3. MitochondrialND1Variants in 1281 Chinese Subjects With Leber's Hereditary Optic Neuropathy

4. Leber's hereditary optic neuropathy: A multifactorial disease

Cited by 6 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. Mitochondrial DNA variants in a cohort from Argentina with suspected Leber’s hereditary optic neuropathy (LHON);PLOS ONE;2023-02-24

2. Analysis of Human Clinical Mutations of Mitochondrial ND1 in a Bacterial Model System for Complex I;Life;2022-11-20

3. A Case of a 23-Year-Old Male With Leber Hereditary Optic Neuropathy With a Rare Mutation;Cureus;2022-10-11

4. Foveal pit morphological changes in asymptomatic carriers of the G11778A mutation with Leber’s hereditary optic neuropathy;International Journal of Ophthalmology;2020-05-18

5. Mutation m.3395A > G in MT-ND1 leads to variable pathologic manifestations;Human Molecular Genetics;2020-02-03

同舟云学术

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