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Glutaric aciduria; Presence of glutaconic and β-hydroxyglutaric acids in urine

✍ Scribed by Oddvar Stokke; Stephen I. Goodman; John A. Thompson; Barbara S. Miles

Book ID
115766431
Publisher
Elsevier Science
Year
1975
Tongue
English
Weight
312 KB
Volume
12
Category
Article
ISSN
0006-2944

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On the neurotoxicity of glutaric, 3-hydr
On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1
✍ T.M. Lund; E. Christensen; A.S. Kristensen; A. Schousboe; A.M. Lund 📂 Article 📅 2004 🏛 John Wiley and Sons 🌐 English ⚖ 142 KB

## Abstract Glutaric acidemia type 1 (GA1) is an autosomal recessively inherited deficiency of glutaryl‐CoA dehydrogenase. Accumulating metabolites, 3‐hydroxyglutaric (3‐OH‐GA), glutaric (GA), and __trans__‐glutaconic (TG) acids, have been proposed to be involved in the development of the striatal