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Abstract
Entities: Disease
Mesh: See more » Adrenal Hyperplasia, Congenital/diagnosisAmino Acid Metabolism, Inborn Errors/diagnosisCarrier StateCeruloplasminCholinesterasesCystic Fibrosis/diagnosisDiagnostic ServicesFemaleGalactosemias/diagnosisGenetic Diseases, Inborn/diagnosisHepatolenticular Degeneration/diagnosisHumansInfantInfant, NewbornMaleMaple Syrup Urine Disease/diagnosisMetabolism, Inborn Errors/diagnosisPhenylketonurias/diagnosisPorphyrias/diagnosisTyrosine/bloodWorld Health Organization
Substances: See more » TyrosineCeruloplasminCholinesterases
Year: 1968 PMID: 4973455
Source DB: PubMed Journal: World Health Organ Tech Rep Ser ISSN: 0512-3054