M M Thaler, N J Hoogenraad, M Boswell. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh: See more » Ammonia/bloodBrain Diseases/etiologyChildFatty Liver/etiologyFemaleHepatic Encephalopathy/pathologyHumansKineticsLiver/pathologyMetabolism, Inborn Errors/complicationsOrnithine/metabolismOrnithine Carbamoyltransferase/metabolismProthrombin TimeReye Syndrome/enzymologyReye Syndrome/etiologyReye Syndrome/pathologyUrea/blood
Substances: See more » AmmoniaUreaOrnithineOrnithine Carbamoyltransferase
Year: 1974 PMID: 4137171 DOI: 10.1016/s0140-6736(74)91819-4
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321