Homocystinuria caused by 5,10-methylenetetrahydrofolate reductase deficiency: A case in an infant responding to methionine, folinic acid, pyridoxine, and vitamin B12 therapy
- 28 February 1981
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 98 (2) , 275-278
- https://doi.org/10.1016/s0022-3476(81)80660-9
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Folate Distribution in Cultured Human CellsJournal of Clinical Investigation, 1979
- Methylenetetrahydrofolate Reductase in Cultured Human Cells. II. Genetic and Biochemical Studies of Methylenetetrahydrofolate Reductase DeficiencyPediatric Research, 1977
- Methylenetetrahy drofolate Reductase in Cultured Human Cells. I. Growth and Metabolic StudiesPediatric Research, 1977
- Morphologic Studies in a Patient with Homocystinuria due to 5,10-Methylenetetrahydrofolate Reductase DeficiencyPediatric Research, 1976
- Homocystinuria associated with decreased methylenetetrahydrofolate reductase activityBiochemical and Biophysical Research Communications, 1972
- Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.Archives of Disease in Childhood, 1967
- Automatic Recording Apparatus for Use in Chromatography of Amino AcidsAnalytical Chemistry, 1958