Ornithine transcarbamylase deficiency presenting with strokelike episodes
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference10 articles.
1. Urea cycle enzymes;Brusilow,1989
2. Lateonset ornithine transcarbamylase deficiency in male patients;Finkelstein;J Pediatr,1990
3. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J Pediatr,1986
4. Retrospective survey of urea cycle disorders. II. Neurological outcome in fortynine Japanese patients with urea cycle enzymopathies;Nagata;Am J Med Genet,1991
5. Study of enzyme defect in a case of ornithine transcarbamylase deficiency;Qureshi;Diabete Metab,1978
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