## Abstract GlutarylโCoA dehydrogenase deficiency is an inherited organic aciduria with predominantly neurological presentation. Biochemically, it is characterized by an accumulation and enhanced urinary excretion of two key organic acids, glutaric acid and 3โhydroxyglutaric acid. If untreated, acu
โฆ LIBER โฆ
Biochemistry and bioenergetics of glutaryl-CoA dehydrogenase deficiency
โ Scribed by S. W. Sauer
- Publisher
- Springer
- Year
- 2007
- Tongue
- English
- Weight
- 431 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0141-8955
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