The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations

Published:2010-08 Issue:2 Volume:399 Page:179-185
ISSN:0006-291X
Container-title:Biochemical and Biophysical Research Communications
language:en
Short-container-title:Biochemical and Biophysical Research Communications

Author:

Zou Yang,Jia Xiaoyun,Zhang A-Mei,Wang Wen-Zhi,Li Shiqiang,Guo Xiangming,Kong Qing-Peng,Zhang Qingjiong,Yao Yong-Gang

Funder

National Natural Science Foundation of China

Yunnan Province

Guangdong Province

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference32 articles.

1. Mitochondrial dysfunction as a cause of optic neuropathies;Carelli;Prog. Retin. Eye Res.,2004

2. Inherited mitochondrial optic neuropathies;Yu-Wai-Man;J. Med. Genet.,2009

3. Leber’s hereditary optic neuropathy: a multifactorial disease;Yen;Prog. Retin. Eye Res.,2006

4. Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background;Hudson;Am. J. Hum. Genet.,2007

5. Mitochondrial DNA haplogroups M7b1’2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G>A mutation;Ji;Am. J. Hum. Genet.,2008

Cited by 27 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 complex I subunit MT-ND1 mutations affect disease progression;Heliyon;2024-04

2. Variability of the mitochondrial genome in young Yakut patients with breast cancer;Siberian journal of oncology;2024-01-03

3. De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome;Gene;2023-04

4. Genetic differentiation of Andaman Islanders and their relatedness to Nicobar Islanders;Human Gene;2023-02

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

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