Ornithine carbamoyltransferase deficiency. A new variant with subnormal enzyme activity

Author:

Rabier D.,Benoit A.,Petit F.,Chekoury A.,Bonnefont J.P.,Saudubray J.M.,Kamoun P.

Publisher

Elsevier BV

Subject

Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine

Reference9 articles.

1. Urea cycle disorders and other hereditary hyperammonemic syndromes;Walser,1983

2. Ornithine transcarbamoylase deficiencies in human males. Kinetic and immunochemical classification;Briand;Biochim Biophys Acta,1982

3. The effects of pH on the kinetics of human liver ornithine carbamoylphosphate transferase;Snodgrass;Biochemistry,1968

4. Catalytic acceleration of the urea diacetyl monoxime phenazone reaction and its application to automatic analysis;Ceriotti;Clin Chim Acta,1965

5. Multiple assays of the five urea-cycle enzymes in human liver homogenates;Nuzum,1976

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