Inborn errors of pyruvate metabolism
Copyright policy )Inborn errors of pyruvate metabolism
- University of Toronto Canada
- Hospital for Sick Children Canada
Methylmalonyl-CoA Decarboxylase, L-Lactate Dehydrogenase, Carboxy-Lyases, Biotin, Ketone Oxidoreductases, Pyruvate Dehydrogenase Complex, Dihydrolipoyllysine-Residue Acetyltransferase, 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide), Pyruvate Carboxylase Deficiency Disease, Ligases, Carbon-Carbon Ligases, Acetyltransferases, Multienzyme Complexes, Humans, Pyruvates, Pyruvate Dehydrogenase Complex Deficiency Disease, Cells, Cultured, Dihydrolipoamide Dehydrogenase
Methylmalonyl-CoA Decarboxylase, L-Lactate Dehydrogenase, Carboxy-Lyases, Biotin, Ketone Oxidoreductases, Pyruvate Dehydrogenase Complex, Dihydrolipoyllysine-Residue Acetyltransferase, 3-Methyl-2-Oxobutanoate Dehydrogenase (Lipoamide), Pyruvate Carboxylase Deficiency Disease, Ligases, Carbon-Carbon Ligases, Acetyltransferases, Multienzyme Complexes, Humans, Pyruvates, Pyruvate Dehydrogenase Complex Deficiency Disease, Cells, Cultured, Dihydrolipoamide Dehydrogenase
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