Glutaric acidemia type II: Clinical, biochemical, and morphologic considerations
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Abstract
References (17)
Glutaric aciduria type II: Report on a previously undescribed metabolic disorder
1976 • 229 citations
L‐2‐Hydroxyglutaric aciduria: an inborn error of metabolism?
1980 • 216 citations
Glutaric aciduria Type II
1980 • 214 citations
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1977 • 210 citations
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1977 • 196 citations
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1981 • 143 citations
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1981 • 140 citations
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1980 • 133 citations
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1982 • 115 citations
Glutaric acidemia
1980 • 113 citations
The purification and some properties of electron transfer flavoprotein and general fatty acyl coenzyme A dehydrogenase from pig liver mitochondria.
1975 • 112 citations
Multiple Acyl-CoA Dehydrogenase Deficiency (Glutaric Aciduria Type II) with Transient Hypersarcosinemia and Sarcosinuria; Possible Inherited Deficiency of an Electron Transfer Flavoprotein
1980 • 97 citations
The oxidation of <scp>d</scp>-α-hydroxy acids in animal tissues
1961 • 83 citations
Biochemical studies in a patient with defects in the metabolism of acyl‐CoA and sarcosine: Another possible case of glutaric aciduria type II
1980 • 63 citations
Glutaric Aciduria Type II. In Vitro Studies on Substrate Oxidation, Acyl-CoA Dehydrogenases, and Electron-Transferring Flavoprotein in Cultured Skin Fibroblasts
1980 • 38 citations
Human mitochondrial electron transport chain: Assay of succinate:Cytochrome c reductase in leukocytes, platelets and cultured fibroblasts
1981 • 33 citations
The Electron-transferring Flavoprotein as a Common Intermediate in the Mitochondrial Oxidation of Butyryl Coenzyme A and Sarcosine
1966 • 32 citations