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Pyruvate Dehydrogenase Complex Deficiency due to a De Novo Heterozygous Mutation in Exon 7 of PDHA 1 Gene Presenting as Isolated Severe Lactic Acidosis in an Infant: Correspondence

Crossref DOI link: https://doi.org/10.1007/s12098-020-03473-y

Published Online: 2020-08-18

Published Print: 2021-04

Update policy: https://doi.org/10.1007/springer_crossmark_policy

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