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Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families. [electronic resource] by
- Zhang, Juanjuan
- Zhou, Xiangtian
- Zhou, Jian
- Li, Chengwu
- Zhao, Fuxin
- Wang, Yan
- Meng, Yanzi
- Wang, Jiying
- Yuan, Meixia
- Cai, Wanshi
- Tong, Yi
- Sun, Yan-Hong
- Yang, Li
- Qu, Jia
- Guan, Min-Xin
Producer: 20101007
In:
Biochemical and biophysical research communications vol. 399
Availability: No items available.
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Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation. [electronic resource] by
- Zhang, Minglian
- Zhou, Xiangtian
- Li, Chengwu
- Zhao, Fuxin
- Zhang, Juanjuan
- Yuan, Meixia
- Sun, Yan-Hong
- Wang, Jingzheng
- Tong, Yi
- Liang, Min
- Yang, Li
- Cai, Wanshi
- Wang, Lifei
- Qu, Jia
- Guan, Min-Xin
Producer: 20110127
In:
Molecular genetics and metabolism vol. 101
Availability: No items available.
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Leber's hereditary optic neuropathy is associated with the T12338C mutation in mitochondrial ND5 gene in six Han Chinese families. [electronic resource] by
- Liu, Xiao-Ling
- Zhou, Xiangtian
- Zhou, Jian
- Zhao, Fuxin
- Zhang, Juanjuan
- Li, Chengwu
- Ji, Yanchun
- Zhang, Yu
- Wei, Qi-Ping
- Sun, Yan-Hong
- Yang, Li
- Lin, Bing
- Yuan, Yumin
- Li, Yingzi
- Qu, Jia
- Guan, Min-Xin
Producer: 20110708
In:
Ophthalmology vol. 118
Availability: No items available.
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