Hyperammonämien
Author:
Publisher
Springer Berlin Heidelberg
Link
http://link.springer.com/content/pdf/10.1007/978-3-662-09176-0_37
Reference7 articles.
1. Bachmann C (1992) Ornithine carbamoyltransferase deficiency: findings, models and problems. J Inher Metab Dis 15: 578–591
2. Bachmann C (1998) Satellite Meeting on Advances in Inherited Urea Cycle Disorders. Recent results — new questions. J Inher Metab Dis 21/11:1–5
3. Feillet F, Leonard JV (1998) Alternative pathway therapy for urea cycle disorders. J Inher Metab Dis 21/1:101–111
4. Msall M, Batshaw ML, Suss R, Brusilow SWMelits ED, (1984) Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea cycle enzymopathies. N Engl J Med 310:1500–1505
5. Summar ML (1998) Molecular genetic research into carbamoyl-phosphate synthase I: Molecular defect and linkage markers. J Inher Metab Dis 21/1: 30–39
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