Genetic analysis in a cohort of patients with hereditary optic neuropathies in Southwest of China

Author:

Guo Hong,Li Shiying,Dai Limeng,Huang Xiaoyong,Yu Tao,Yin Zhengqin,Bai Yun

Funder

National Natural Science Foundation of China

Natural Science Foundation Project of CQ CSTC

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Molecular Medicine

Reference38 articles.

1. A gene for X-linked optic atrophy is closely linked to the Xp11.4-Xp11.2 region of the X chromosome;Assink;Am. J. Hum. Genet.,1997

2. Exaggerated status of "novel" and "pathogenic" mtDNA sequence variants due to inadequate database searches;Bandelt;Hum. Mutat.,2009

3. A first locus for isolated autosomal recessive optic atrophy (ROA1) maps to chromosome 8q;Barbet;Eur. J. Hum. Genet.,2003

4. A third locus for dominant optic atrophy on chromosome 22q;Barbet;J. Med. Genet.,2005

5. Complete mitochondrial DNA genome sequence variation of Chinese families with mutation m.3635G>a and Leber hereditary optic neuropathy;Bi;Mol. Vis.,2012

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