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
โฆ LIBER โฆ
Lactate Dehydrogenase Activity is Inhibited by Methylmalonatein vitro
โ 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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