Ornithine carbamoyl transferase deficiency: Findings, models and problems

Author:

Bachmann C.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference40 articles.

1. Bachmann C (1974) Urea cycle. In Nyhan WL, ed.Heritable Disorders of Aminoacid Metabolism. New York: Wiley, 361–386.

2. Bachmann C (1983) Brain tryptophan uptake and glutamine synthetase in hyperammonemic rats.Hoppe Seyler's Z Physiol Chem 364: 1255–1256.

3. Bachmann C (1987) Diagnosis of urea cycle disorders.Enzyme 38: 233–241.

4. Bachmann C (1990) Urea cycle disorders. In Fernandes J, Saudubray JM, Tada K, eds.Inborn Metabolic Diseases. Berlin: Springer, 211–228.

5. Bachmann C, Colombo JP (1981) Computer simulation of the urea cycle: Trials for an appropriate model.Enzyme 26: 259–264.

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