Fabry's disease: evidence for a physically altered -galactosidase.
- 1 May 1972
- journal article
- Vol. 24 (3) , 256-66
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Biochemical and electrophoretic studies of -galactosidase in normal man, in patients with Fabry's disease, and in Equidae.1972
- Adult Gaucher's disease: kindred studies and demonstration of a deficiency of acid beta-glucosidase in cultured fibroblasts.1972
- Gaucher's Disease: Deficiency of “cid”β-Glucosidase and Reconstitution of Enzyme Activity In VitroProceedings of the National Academy of Sciences, 1971
- Differential effect of chloride ions on β-galactosidase isoenzymes: A method for separate assayClinica Chimica Acta; International Journal of Clinical Chemistry, 1971
- Lysosomal hydrolases: Conversion of acidic to basic forms by neuraminidaseFEBS Letters, 1971
- Genetic Inactivation of the α-Galactosidase Locus in Carriers of Fabry's DiseaseScience, 1970
- Fabry's Disease: Alpha-Galactosidase DeficiencyScience, 1970
- Tissue distribution of glycosphingolipids in a case of Fabry's disease.1969
- Enzymatic Defect in Fabry's DiseaseNew England Journal of Medicine, 1967