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Lactate Dehydrogenase Activity is Inhibited by Methylmalonatein vitro

โœ Scribed by Laura O. Saad; Sandra R. Mirandola; Evelise N. Maciel; Roger F. Castilho


Book ID
106483412
Publisher
Springer
Year
2006
Tongue
English
Weight
241 KB
Volume
31
Category
Article
ISSN
0364-3190

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Methylmalonic acidemia (MMAemia) is an inherited metabolic disorder of branched amino acid and odd-chain fatty acid metabolism, involving a defect in the conversion of methylmalonyl-coenzyme A to succinylcoenzyme A. Systemic and neurological manifestations in this disease are thought to be associate

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