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

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

DOI Full Paper Access

102

Citations

15

References

1980

Year

Stephen I. Goodman, Edward R.B. McCabe, Paul V. Fennessey, John Mace

Pediatric Research

Possible Inherited DeficiencyElectron Transfer FlavoproteinMetabolic DisorderBiochemistryPathologyTransient HypersarcosinemiaMetabolismMedicineOxidative Stress

References

	Year	Citations

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