✦ LIBER ✦

The mitochondrial tRNAGlu A14693G mutation may influence the phenotypic manifestation of ND1 G3460A mutation in a Chinese family with Leber’s hereditary optic neuropathy

✍ Scribed by Yi Tong; Yijian Mao; Xiangtian Zhou; Li Yang; Juanjuan Zhang; Wanshi Cai; Fuxing Zhao; Xinjian Wang; Fan Lu; Jia Qu; Min-Xin Guan

No coin nor oath required. For personal study only.

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Mitochondrial variants may influence the

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Mitochondrial tRNAGlu A14693G variant ma

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Very low penetrance of Leber’s hereditar

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Leber’s hereditary optic neuropathy is a

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Only male matrilineal relatives with Leb

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The mitochondrial tRNAThr A15951G mutati

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