## Abstract ## Background Methylmalonic aciduria is an autosomal recessive inborn error of the propionate metabolic pathway. One form of this disorder is caused by mutations in methylmalonylโcoenzyme A mutase (MCM), resulting in reduced levels of enzyme activity. The pharmacological upโregulation
โฆ LIBER โฆ
Induction of methylmalonic aciduria with streptozotocin: A possible experimental model for the study of methylmalonic acidaemia
โ Scribed by H. R. Bhatt; J. C. Linnell
- Publisher
- Springer
- Year
- 1983
- Tongue
- English
- Weight
- 517 KB
- Volume
- 6
- Category
- Article
- ISSN
- 0141-8955
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