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Novel Mitochondrial C15620A Variant may Modulate the Phenotype of Mitochondrial G11778A Mutation in a Chinese Family with Leigh Syndrome

✍ Scribed by Ji, Kunqian; Zheng, Jinfan; Sun, Baoying; Liu, Fuchen; Shan, Jingli; Li, Duoling; Luo, Yue-Bei; Zhao, Yuying; Yan, Chuanzhu

No coin nor oath required. For personal study only.

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