Unusual biochemical and clinical features in a girl with ornithine transcarbamylase deficiency
- 1 January 1986
- journal article
- case report
- Published by Elsevier in Pediatric Neurology
- Vol. 2 (1) , 51-53
- https://doi.org/10.1016/0887-8994(86)90041-x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
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- Treatment of Carbamyl Phosphate Synthetase Deficiency with Keto Analogues of Essential Amino AcidsNew England Journal of Medicine, 1975
- Evidence for X-Linked Dominant Inheritance of Ornithine Transcarbamylase DeficiencyNew England Journal of Medicine, 1973
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- HEREDITARY HYPERAMMONÆMIABrain, 1970