J Amir, G Alpert, M Statter, A Gutman, S H Reisner. Show Affiliations »
Abstract
Entities: Disease Gene
Mesh： See more » Amino Acid Metabolism, Inborn Errors/geneticsAmmonia/bloodCerebral Hemorrhage/geneticsHumansInfant, NewbornInfant, Newborn, DiseasesMaleOrnithine Carbamoyltransferase Deficiency Disease
Substances： See more » Ammonia
Year: 1982 PMID： 7136688 DOI： 10.1111/j.1651-2227.1982.tb09497.x
Source DB: PubMed Journal: Acta Paediatr Scand ISSN： 0001-656X