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The coexistence of mitochondrial ND6 T14484C and 12S rRNA A1555G mutations in a Chinese family with Leber’s hereditary optic neuropathy and hearing loss

✍ Scribed by Qi-Ping Wei; Xiangtian Zhou; Li Yang; Yan-Hong Sun; Jian Zhou; Guang Li; Robert Jiang; Fan Lu; Jia Qu; Min-Xin Guan

No coin nor oath required. For personal study only.

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