The electrophoretic separation of human β-galactosidases on cellulose acetate
- 30 April 1971
- journal article
- Published by Elsevier in Biochemical Medicine
- Vol. 5 (2), 158-164
- https://doi.org/10.1016/0006-2944(71)90083-4
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- G M1 ‐gangliosidosis without chondrodystrophy or visceromegalyNeurology, 1970
- β-Galactosidase in Tissue Culture Derived from Human Skin and Bone Marrow: Enzyme defect in GM1 GangliosidosisPediatric Research, 1969
- Beta-Galactosidase Deficiency in the Hurler SyndromeNew England Journal of Medicine, 1969
- Hurler's Syndrome: Deficiency of a Specific Beta Galactosidase IsoenzymeScience, 1969
- The Abnormalities of Lysosomal Enzymes in MucopolysaccharidosesEuropean Journal of Biochemistry, 1968
- GLYCOSIDASES IN SKIN AND PLASMA IN HUNTER'S SYNDROME Abnormality of a β‐galactosidase in SkinActa Paediatrica, 1968
- Generalized Gangliosidosis: Beta-Galactosidase DeficiencyScience, 1968
- Acid hydrolases in skin and plasma in gargoylism. Deficiency of β-galactosidase in skinClinica Chimica Acta; International Journal of Clinical Chemistry, 1968
- Lysosomal Acid Hydrolases in the Liver in Gargoylism Deficiency of 4-methylumbelliferyl-β-galactosidaseScandinavian Journal of Clinical and Laboratory Investigation, 1968
- Separation and properties of β-galactosidase, β-glucosidase, β-glucuronidase and N-acetyl-β-glucosaminidase from rat kidneyBiochemical Journal, 1967