R H Glew, A Basu, E M Prence, A T Remaley. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Arylsulfatases/deficiencyCystine/metabolismFabry Disease/enzymologyFabry Disease/geneticsG(M1) Ganglioside/metabolismG(M2) Ganglioside/metabolismGalactosylceramidase/metabolismGangliosidoses/physiopathologyGenetic Carrier ScreeningGlycoproteins/metabolismHeparitin Sulfate/metabolismHumansHydrolases/deficiencyIsoelectric FocusingIsoenzymes/metabolismKineticsLeukodystrophy, Globoid Cell/geneticsLeukodystrophy, Metachromatic/physiopathologyLipid Metabolism, Inborn Errors/geneticsLipid Metabolism, Inborn Errors/metabolismLysosomes/enzymologyMetabolism, Inborn Errors/enzymologyMetabolism, Inborn Errors/physiopathologyMolecular WeightMucolipidoses/metabolismNiemann-Pick Diseases/enzymologySphingolipidoses/physiopathologySphingomyelin Phosphodiesterase/metabolismalpha-Galactosidase/geneticsalpha-Galactosidase/metabolismbeta-Galactosidase/metabolism
Substances: See more » GlycoproteinsIsoenzymesG(M2) GangliosideG(M1) GangliosideCystineHeparitin SulfateHydrolasesSphingomyelin PhosphodiesteraseArylsulfatasesalpha-Galactosidasebeta-GalactosidaseGalactosylceramidase
Year: 1985 PMID: 2993742
Source DB: PubMed Journal: Lab Invest ISSN: 0023-6837 Impact factor: 5.662