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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.

Indian journal of pediatrics - 1 Jan 2021

Ganesh Ramaswamy, Suresh Natarajan, Vasuki B, Narayanan Karthik

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Share to Acidosis, Lactic
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Pyruvate Dehydrogenase (Lipoamide)

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PMID: 32537710
DOI: 10.1007/s12098-020-03394-w

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