中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
机构
采集方式
内容类型
发表日期
学科主题
筛选

浏览/检索结果: 共3条,第1-3条 帮助

条数/页: 排序方式:
The MT-ND1 and MT-ND5 genes are mutational hotspots for Chinese families with clinical features of LHON but lacking the three primary mutations 期刊论文  OAI收割
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2010, 卷号: 399, 期号: 2, 页码: 179-185
作者:  
Zou Y;  Jia XY;  Zhang AM;  Wang WZ;  Li SQ
收藏  |  浏览/下载:20/0  |  提交时间:2010/10/28
Co-occurrence of a1555g and g11778a in a chinese family with high penetrance of leber's hereditary optic neuropathy 期刊论文  iSwitch采集
Biochemical and biophysical research communications, 2008, 卷号: 376, 期号: 1, 页码: 221-224
作者:  
Zhang, A-Mei;  Jia, Xiaoyun;  Yao, Yong-Gang;  Zhang, Qingjiong
收藏  |  浏览/下载:26/0  |  提交时间:2019/05/10
Co-occurrence of A1555G and G11778A in a Chinese family with high penetrance of Leber's hereditary optic neuropathy 期刊论文  OAI收割
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2008, 卷号: 376, 期号: 1, 页码: 221-224
作者:  
Zhang AM;  Jia XY;  Yao YG[*];  Zhang QJ[*]
收藏  |  浏览/下载:16/0  |  提交时间:2010/08/24