A new variant of methylmalonic acidemia-defective coenzyme-apoenzyme binding in cultured fibroblasts
- 3 April 1978
- journal article
- case report
- Published by Elsevier in Clinica Chimica Acta; International Journal of Clinical Chemistry
- Vol. 85 (1) , 67-72
- https://doi.org/10.1016/0009-8981(78)90102-x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- Methylmalonic aciduria: A variant form of methylmalonyl coenzyme A apomutase deficiencyThe Journal of Pediatrics, 1977
- Methylmalonic Aciduria without Vitamin B12Deficiency in an Adult SibshipNew England Journal of Medicine, 1976
- Studies of methylmalonyl-coenzyme A carbonylmutase activity in methylmalonic acidemiaBiochemical Medicine, 1976
- Studies of Methylmalonyl Coenzyme A Carbonylmutase Activity in Methylmalonic Acidemia. I. Correlation of Clinical, Hepatic, and Fibroblast DataPediatric Research, 1975
- In vitro “responsive” methylmalonic acidemia: A new variantThe Journal of Pediatrics, 1974
- Methylmalonyl Coenzyme A Racemase Defect: Another Cause of Methylmalonic AciduriaPediatric Research, 1972
- A derangement in B12 metabolism associated with homocystinemia, cystathioninemia, hypomethioninemia and methylmalonic aciduriaThe American Journal of Medicine, 1970
- Studies in a patient with methylmalonic acidemiaThe Journal of Pediatrics, 1969
- Methylmalonic Aciduria: Metabolic Block Localization and Vitamin B 12 DependencyScience, 1968
- Methylmalonic aciduria. An inborn error of metabolism leading to chronic metabolic acidosis.Archives of Disease in Childhood, 1967