Transient 5‐oxoprolinuria in a very low‐birthweight infant
- 1 March 1992
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (2) , 284-285
- https://doi.org/10.1007/bf01799646
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- 5‐OXOPROLINURIA DUE TO HEREDITARY 5‐OXOPROLINASE DEFICIENCY IN TWO BROTHERS–A NEW INBORN ERROR OF THE γ‐GLUTAMYL CYCLEActa Paediatrica, 1981
- 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