Y Wada, K Narisawa, T Arakawa. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Apnea/geneticsBrain/enzymologyConsanguinityFemaleGenes, RecessiveGenetic Carrier ScreeningHomocystinuria/geneticsHomozygoteHumansInfantInfant, NewbornInfant, Newborn, Diseases/geneticsIntellectual Disability/geneticsKidney/enzymologyLeukocytes/enzymologyLiver/enzymologyMethylenetetrahydrofolate Dehydrogenase (NADP)/deficiencyOxidoreductases/deficiencySeizures/geneticsSyndrome
Substances: See more » OxidoreductasesMethylenetetrahydrofolate Dehydrogenase (NADP)
Year: 1978 PMID: 732831 DOI: 10.1159/000401626
Source DB: PubMed Journal: Monogr Hum Genet ISSN: 0077-0876