Late-onset ornithine transcarbamylase deficiency in male patients
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology and Child Health
Reference24 articles.
1. Urea cycle enzymes;Brusilow,1989
2. Natural history of symptomatic partial ornithine transcarbamylase deficiency;Rowe;N Engl J Med,1986
3. Risk of serious illness in heterozygotes for ornithine transcarbamylase deficiency;Batshaw;J Pediatr,1986
4. Episodes of hyperammonemic coma, often postpartum, occurring in women who have a mutation at the ornithine transcarbamylase locus;Arn;N Engl J Med,1990
5. Hyperammonemia: a variant type of liver ornithine transcarbamylase;Levin;Arch Dis Child,1969
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