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Pyruvate dehydrogenase e3-binding protein deficiency

Diaphorase deficiencyDihydrolipoyl dehydrogenase deficiencyGlycine cleavage system L protein deficiencyPyruvate dehydrogenase protein X component deficiencyLipoamide dehydrogenase deficiency2-oxoglutarate complex deficiencyBranched chain alpha-ketoacid dehydrogenase complex deficiency
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Type of Disease: Genetic, autosomal recessive Pediatric onset

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