Results
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Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation. [electronic resource] by
- Liang, Min
- Guan, Minqiang
- Zhao, Fuxing
- Zhou, Xiangtian
- Yuan, Meixia
- Tong, Yi
- Yang, Li
- Wei, Qi-Ping
- Sun, Yan-Hong
- Lu, Fan
- Qu, Jia
- Guan, Min-Xin
Producer: 20090511
In:
Biochemical and biophysical research communications vol. 383
Availability: No items available.
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Leber's hereditary optic neuropathy is associated with mitochondrial ND6 T14502C mutation. [electronic resource] by
- Zhao, Fuxin
- Guan, Minqiang
- Zhou, Xiangtian
- Yuan, Meixia
- Liang, Ming
- Liu, Qi
- Liu, Yan
- Zhang, Yongmei
- Yang, Li
- Tong, Yi
- Wei, Qi-Ping
- Sun, Yan-Hong
- Qu, Jia
- Guan, Min-Xin
Producer: 20091113
In:
Biochemical and biophysical research communications vol. 389
Availability: No items available.
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5.
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The ND4 G11696A mutation may influence the phenotypic manifestation of the deafness-associated 12S rRNA A1555G mutation in a four-generation Chinese family. [electronic resource] by
- Liao, Zhisu
- Zhao, Jianyue
- Zhu, Yi
- Yang, Li
- Yang, Aifen
- Sun, Dongmei
- Zhao, Zhongnong
- Wang, Xinjian
- Tao, Zhihua
- Tang, Xiaowen
- Wang, Jindan
- Guan, Minqiang
- Chen, Jiafu
- Li, Zhiyuan
- Lu, Jianxin
- Guan, Min-Xin
Producer: 20071101
In:
Biochemical and biophysical research communications vol. 362
Availability: No items available.
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Mitochondrial ND5 T12338C, tRNA(Cys) T5802C, and tRNA(Thr) G15927A variants may have a modifying role in the phenotypic manifestation of deafness-associated 12S rRNA A1555G mutation in three Han Chinese pedigrees. [electronic resource] by
- Chen, Bobei
- Sun, Dongmei
- Yang, Li
- Zhang, Chuqin
- Yang, Aifen
- Zhu, Yi
- Zhao, Jianyue
- Chen, Yingying
- Guan, Minqiang
- Wang, Xinjian
- Li, Ronghua
- Tang, Xiaowen
- Wang, Jindan
- Tao, Zhihua
- Lu, Jianxin
- Guan, Min-Xin
Producer: 20080528
In:
American journal of medical genetics. Part A vol. 146A
Availability: No items available.
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