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    Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy

    Clinical exome sequencing reveals a mutation in PDHA1 in Leigh syndrome: A case of a Chinese boy with lethal neuropathy by Ke Gong, Li Xie, Zhong‐shi Wu, Xia Xie, Xing‐xing Zhang, Jin‐Lan Chen

    Published 2021-04-01
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