Glutaric Aciduria Type II: Multiple Defects in Isolated Muscle Mitochondria and Deficient β-Oxidation in Fibroblasts

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

P. G. Barth, H.R. Scholte, J.A. Berden et al. · Journal of the Neurological Sciences · 1983 · 701 citations

Medicine, Cardiology, Molecular Genetics +17

Multiple Acyl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type II) with Transient Hypersarcosinemia and Sarcosinuria; Possible Inherited Deficiency of an Electron Transfer Flavoprotein

Stephen I. Goodman, Edward R.B. McCabe, Paul V. Fennessey et al. · Pediatric Research · 1980 · 102 citations

Life Sciences, Biochemistry, Molecular Genetics +13

Mammalian Metabolism of Glutaric Acid

A Besrat, C.E. Polan, L.M. Henderson · Journal of Biological Chemistry · 1969 · 96 citations · Full text

Life Sciences, Biochemistry, Cellular Metabolism +11

Glutaric Aciduria Type II. In Vitro Studies on Substrate Oxidation, Acyl-CoA Dehydrogenases, and Electron-Transferring Flavoprotein in Cultured Skin Fibroblasts

William J. Rhead, S Mantagos, Kay Tanaka · Pediatric Research · 1980 · 37 citations

Life Sciences, Biochemistry, Cell Biology +9

Liver malonyl-CoA decarboxylase

H.R. Scholte · Biochimica et Biophysica Acta (BBA) - Enzymology · 1973 · 16 citations