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ArticleMolecular genetics & genomic medicine2021

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

Ke Gong et al.PubMed ↗Full text ↗Publisher ↗

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2021
2022
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Full record →Abstract, authors, funding and every citing paper · PMID 33661577