A Neetens, K J Van Acker, N Marien. Show Affiliations »
Abstract
Entities: Disease
Mesh： See more » Adenine Phosphoribosyltransferase/deficiencyChildCorneal Dystrophies, Hereditary/etiologyCorneal Dystrophies, Hereditary/geneticsHumansInfantMalePentosyltransferases/deficiencyPurine-Pyrimidine Metabolism, Inborn Errors/complicationsPurine-Pyrimidine Metabolism, Inborn Errors/genetics
Substances： See more » PentosyltransferasesAdenine Phosphoribosyltransferase
Year: 1986 PMID： 3487363
Source DB: PubMed Journal: Bull Soc Belge Ophtalmol ISSN： 0081-0746