Ornithine transcarbamylase deficiency in a boy with normal development
- 31 March 1980
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 96 (3), 441-443
- https://doi.org/10.1016/s0022-3476(80)80694-9
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Atypical Clinical Course of Ornithine Transcarbamyiase Deficiency Due to a New Mutant (Comparison with Reye's Disease)Journal of Clinical Endocrinology & Metabolism, 1979
- Treatment of complete ornithine transcarbamylase deficiency with nitrogen-free analogues of essential amino acidsThe Journal of Pediatrics, 1978
- Evidence for X-Linked Dominant Inheritance of Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1973
- Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1973
- Ornithine carbamyl transferase: The effects of pH on the kinetics of a mutant human enzymeClinica Chimica Acta; International Journal of Clinical Chemistry, 1972
- Hyperammonaemia. A variant type of deficiency of liver ornithine transcarbamylase.Archives of Disease in Childhood, 1969
- HEREDITARY OROTIC ACIDURIAPediatrics, 1968
- Hyperlysinemia Associated with RetardationNew England Journal of Medicine, 1965
- Studies on carbamoyl phosphate-l-ornithine Carbamoyltransferase from ox liverBiochemical Journal, 1963