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Wanshi Cai
Wanshi Cai
Wenzhou Medical College
Haplogroup
Leber's hereditary optic neuropathy
Genetics
Biology
Mutation
4
Papers
119
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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.
2010
Molecular Genetics and Metabolism
Minglian Zhang
Xiangtian Zhou
Chengwu Li
Fuxin Zhao
Juanjuan Zhang
Meixia Yuan
Yan-Hong Sun
Jingzheng Wang
Yi Tong
Min Liang
Li Yang
Wanshi Cai
Lifei Wang
Jia Qu
Min-Xin Guan
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Citations (31)
Mitochondrial ND6 T14502C variant may modulate the phenotypic expression of LHON-associated G11778A mutation in four Chinese families.
2010
Biochemical and Biophysical Research Communications
Juanjuan Zhang
Xiangtian Zhou
Jian Zhou
Chengwu Li
Fuxin Zhao
Yan Wang
Yanzi Meng
Jiying Wang
Meixia Yuan
Wanshi Cai
Yi Tong
Yan-Hong Sun
Li Yang
Jia Qu
Min-Xin Guan
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Citations (20)
Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation.
2008
Journal of Genetics and Genomics
Wanshi Cai
Qun Fu
Xiangtian Zhou
Jia Qu
Yi Tong
Min-Xin Guan
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Citations (42)
The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy
2007
Biochemical and Biophysical Research Communications
Yi Tong
Yijian Mao
Xiangtian Zhou
Li Yang
Juanjuan Zhang
Wanshi Cai
Fuxing Zhao
Xinjian Wang
Fan Lu
Jia Qu
Min-Xin Guan
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Citations (26)
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