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Literature summary for 1.5.5.1 extracted from

  • Goodman, SI; McCabe, ER; Fennessey, PV; Mace, JW
    Multiple acyl-CoA dehydrogenase deficiency (glutaric aciduria type II) with transient hypersarcosinemia and sarcosinuria; possible inherited deficiency of an electron transfer flavoprotein. (1980), Pediatr Res, 14, 12-7.
    View publication on PubMed
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Organism

Organism UniProt Comment Textmining