N W Cheung, J Earl. Show Affiliations »
Abstract
Entities: Disease Mutation
Mesh： See more » AdultAttention Deficit Disorder with Hyperactivity/geneticsDiagnosis, DifferentialDiarrhea/geneticsEpinephrine/geneticsEpinephrine/metabolismFemaleFlushing/geneticsGenetic Diseases, Inborn/complicationsGenetic Diseases, Inborn/diagnosisGenetic Diseases, Inborn/geneticsGenetic Diseases, Inborn/metabolismGenetic TestingHumansMonoamine Oxidase/deficiencyMonoamine Oxidase/geneticsMonoamine Oxidase/metabolismNorepinephrine/geneticsNorepinephrine/metabolismPoint Mutation/geneticsSerotonin/geneticsSerotonin/metabolism
Substances： See more » SerotoninMonoamine OxidaseNorepinephrineEpinephrine
Year: 2001 PMID： 11700166 DOI： 10.1001/archinte.161.20.2503
Source DB: PubMed Journal: Arch Intern Med ISSN： 0003-9926