Pyroglutamic aciduria (5‐Oxoprolinuria) without glutathione synthetase deficiency and with decreased pyroglutamate hydrolase activity
- 1 December 1981
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 4 (1) , 89-90
- https://doi.org/10.1007/bf02263605
Abstract
No abstract availableKeywords
This publication has 4 references indexed in Scilit:
- [Glutathion-synthetase deficiency with 5-oxoprolinuria. Two new cases and a review of the literature (author's transl)].1978
- Glutathione Synthetase Deficiency, an Inborn Error of Metabolism Involving the γ-Glutamyl Cycle in Patients with 5-Oxoprolinuria (Pyroglutamic Aciduria)Proceedings of the National Academy of Sciences, 1974
- The Metabolism of L-Pyroglutamic Acid in Fibroblasts from a Patient with Pyroglutamic Aciduria: The Demonstration of an L-Pyroglutamate Hydrolase SystemScandinavian Journal of Clinical and Laboratory Investigation, 1972
- Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: Applications to mammalian blood and other tissuesAnalytical Biochemistry, 1969