Arginase deficiency in a 12-year-old boy with mild impairment of intellectual function
- 31 March 1986
- journal article
- case report
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 108 (3), 432-435
- https://doi.org/10.1016/s0022-3476(86)80891-5
Abstract
No abstract availableThis publication has 8 references indexed in Scilit:
- Diagnosis and treatment of argininaemia. Characteristics of arginase in human erythrocytes and tissuesJournal of Inherited Metabolic Disease, 1984
- A new French‐Canadian family affected by hyperargininaemiaJournal of Inherited Metabolic Disease, 1983
- Immunologic Studies of Arginase in Tissues of Normal Human Adult and Arginase-Deficient PatientsPediatric Research, 1983
- Hyperargininemia: Effect of ornithine and lysine supplementationThe Journal of Pediatrics, 1983
- Treatment of hyperargininaemia due to arginase deficiency with a chemically defined dietJournal of Inherited Metabolic Disease, 1981
- Immunoautoradiographic detection of proteins after electrophoretic transfer from gels to diazo-paper: analysis of adenovirus encoded proteins.Proceedings of the National Academy of Sciences of the United States of America, 1981
- Hyperargininemia with Arginase DeficiencyPediatric Research, 1979
- THE FREE AMINO ACIDS OF HUMAN SPINAL FLUID DETERMINED BY ION EXCHANGE CHROMATOGRAPHYJournal of Neurochemistry, 1966