Reduced level of glycine cleavage system in the liver of hyperglycinemia patients
- 15 August 1977
- journal article
- Published by Elsevier BV in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 79 (1), 173-181
- https://doi.org/10.1016/0009-8981(77)90475-2
Abstract
No abstract availableKeywords
This publication has 18 references indexed in Scilit:
- Infantile type of homocystinuria with N5,10-methylenetetrahydrofolate reductase defect.The Tohoku Journal of Experimental Medicine, 1977
- Mechanism of reversible glycine cleavage reaction in Arthrobacter globiformisArchives of Biochemistry and Biophysics, 1976
- Glycine metabolism by rat liver mitochondriaArchives of Biochemistry and Biophysics, 1974
- Glycine metabolism by rat liver mitochondriaArchives of Biochemistry and Biophysics, 1974
- Coexistence of Defective Activity in Glycine-Cleavage Reaction and Propionly-CoA Carboxylase in the Liver of a Hyperglycinemic ChildThe Tohoku Journal of Experimental Medicine, 1974
- Glycine metabolism in rat liver mitochondriaArchives of Biochemistry and Biophysics, 1971
- Physiological significance of glycine cleavage system in human liver as revealed by the study of a case of hyperglycinemiaBiochemical and Biophysical Research Communications, 1969
- DEFECTIVE PROPIONATE CARBOXYLATION IN KETOTIC HYPERGLYCINÆMIAThe Lancet, 1969
- Glycine metabolism by rat liver mitochondriaArchives of Biochemistry and Biophysics, 1969
- Hyperglycinemia: A Defect in Glycine Cleavage ReactionThe Tohoku Journal of Experimental Medicine, 1969