H A Simmonds, A Sahota, C F Potter, J S Cameron. Show Affiliations »
Abstract
Entities: Chemical Disease Gene
Mesh: See more » Adenine Phosphoribosyltransferase/deficiencyAdenosine Deaminase/deficiencyChildChromatography, Ion ExchangeElectrophoresisHumansImmunologic Deficiency Syndromes/diagnosisImmunologic Deficiency Syndromes/urineNucleoside Deaminases/deficiencyPentosyltransferases/deficiencyPurine-Nucleoside Phosphorylase/deficiencyPurine-Pyrimidine Metabolism, Inborn Errors/diagnosisPurine-Pyrimidine Metabolism, Inborn Errors/enzymologyPurine-Pyrimidine Metabolism, Inborn Errors/urinePurines/urine
Substances: See more » PurinesPentosyltransferasesPurine-Nucleoside PhosphorylaseAdenine PhosphoribosyltransferaseNucleoside DeaminasesAdenosine Deaminase
Year: 1978 PMID: 108044 DOI: 10.1042/cs0540579
Source DB: PubMed Journal: Clin Sci Mol Med ISSN: 0301-0538