J H Walter, P T Clayton, J V Leonard. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Amino Acid Metabolism, Inborn Errors/enzymologyAmino Acid Metabolism, Inborn Errors/geneticsAmmonia/bloodFemaleGenetic Carrier ScreeningHumansHypoglycemia/enzymologyInfantOxo-Acid-Lyases/deficiencyReye Syndrome/enzymology
Substances: See more » AmmoniaOxo-Acid-Lyases3-hydroxy-3-methylglutaryl-coenzyme A lyase
Year: 1986 PMID: 3099075 DOI: 10.1007/bf01799665
Source DB: PubMed Journal: J Inherit Metab Dis ISSN: 0141-8955 Impact factor: 4.982