A new variant of glutaric aciduria type II: Deficiency of β‐subunit of electron transfer flavoprotein
- 1 September 1990
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 13 (5) , 783-786
- https://doi.org/10.1007/bf01799588
Abstract
No abstract availableKeywords
This publication has 7 references indexed in Scilit:
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- Biosynthesis of electron transfer flavoprotein in a cell-free system and in cultured human fibroblasts. Defect in the alpha subunit synthesis is a primary lesion in glutaric aciduria type II.Journal of Clinical Investigation, 1986
- Deficiency of electron transfer flavoprotein or electron transfer flavoprotein:ubiquinone oxidoreductase in glutaric acidemia type II fibroblasts.Proceedings of the National Academy of Sciences, 1985
- Purification and Properties of Rat Liver Acyl-CoA Dehydrogenases and Electron Transfer Flavoprotein1The Journal of Biochemistry, 1981
- Glutaric aciduria type II: Report on a previously undescribed metabolic disorderClinica Chimica Acta; International Journal of Clinical Chemistry, 1976