Mitochondrial tRNAThr A15951G mutation may not be associated with Leber’s Hereditary Optic Neuropathy-Reference-Cited by-同舟云学术

登录注册会员服务联系我们

Mitochondrial tRNAThr A15951G mutation may not be associated with Leber’s Hereditary Optic Neuropathy

Published:2015-05-22 Issue:4 Volume:27 Page:2323-2325
ISSN:2470-1394
Container-title:Mitochondrial DNA Part A
language:en
Short-container-title:Mitochondrial DNA Part A

Author:

Zhang Xi¹,Yu Shuaishuai²,Tu Yunhai¹,Huang Wenjie³

Affiliation:

1. Department of Ophthalmic Endoscopic Surgery, the Eye Hospital of Wenzhou Medical University, Wenzhou, China,

2. School of Laboratory Medicine and Life Science, Wenzhou Medical University, Wenzhou, China, and

3. Ward 3, The Eye Hospital of Wenzhou Medical University, Wenzhou, China

Publisher

Informa UK Limited

Subject

Genetics,Molecular Biology

Link

https://www.tandfonline.com/doi/pdf/10.3109/19401736.2015.1022763

Reference25 articles.

1. The 9-bp deletion in region V of mtDNA: a risk factor of hearing loss and encephalomyopathy in Caucasian populations?

2. MITOMAP: a human mitochondrial genome database--2004 update

3. The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J

4. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

5. Mitochondrial DNA G10398A polymorphism imparts maternal Haplogroup N a risk for breast and esophageal cancer

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