W L Nyhan. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » AmniocentesisCarboxy-Lyases/deficiencyFemaleGenetic Carrier ScreeningHomocystinuria/complicationsHumansInfant, NewbornIntellectual Disability/etiologyLesch-Nyhan Syndrome/pathologyLysosomes/pathologyMetabolism, Inborn Errors/diagnosisMetabolism, Inborn Errors/diet therapyMetabolism, Inborn Errors/prevention & controlMetabolism, Inborn Errors/therapyMethylmalonyl-CoA DecarboxylaseMethylmalonyl-CoA Mutase/deficiencyMucopolysaccharidoses/pathologyPhenylketonurias/complicationsPregnancyPrenatal DiagnosisPropionates/deficiencyReferral and ConsultationTay-Sachs Disease/pathologyUrea/metabolismVitamins/therapeutic use
Substances： See more » PropionatesVitaminsUreaCarboxy-LyasesMethylmalonyl-CoA MutaseMethylmalonyl-CoA Decarboxylase
Year: 1980 PMID： 6113913
Source DB: PubMed Journal: Clin Symp ISSN： 0009-9295