
doi: 10.1007/bf01799447
pmid: 3018357
AbstractPyruvate dehydrogenase deficiency may be a non‐specific consequence of many different neurological degenerative disorders. There are also serious methodological problems in estimating the activity of this enzyme complex.
Movement Disorders, Cranial Nerves, Brain, Carbon Dioxide, Dihydrolipoyllysine-Residue Acetyltransferase, NAD, Facial Bones, Feedback, Molecular Weight, Acetyl Coenzyme A, Acetyltransferases, Child, Preschool, Lactates, Humans, Coenzyme A, Lactic Acid, Leigh Disease, Acidosis, Child, Dihydrolipoamide Dehydrogenase
Movement Disorders, Cranial Nerves, Brain, Carbon Dioxide, Dihydrolipoyllysine-Residue Acetyltransferase, NAD, Facial Bones, Feedback, Molecular Weight, Acetyl Coenzyme A, Acetyltransferases, Child, Preschool, Lactates, Humans, Coenzyme A, Lactic Acid, Leigh Disease, Acidosis, Child, Dihydrolipoamide Dehydrogenase
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