Investigation of the α‐Galactosidase Deficiency in Fabry's Disease Using Antibodies against the Purified Enzyme
Open Access
- 1 July 1974
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 46 (1), 89-98
- https://doi.org/10.1111/j.1432-1033.1974.tb03600.x
Abstract
No abstract availableKeywords
This publication has 24 references indexed in Scilit:
- CAVEAT TO PROTEIN REPLACEMENT THERAPY FOR GENETIC DISEASE: IMMUNOLOGICAL IMPLICATIONS OF ACCURATE MOLECULAR DIAGNOSISThe Lancet, 1973
- Hexosaminidase-A and Hexosamini-dase-B: Studies in Tay-Sachs' and Sandhoff's DiseaseNature, 1973
- Rodent and Human Acid α‐GlucosidaseEuropean Journal of Biochemistry, 1972
- Detection and properties of an acid α-galactosidase (ceramidetrihexosidase) in normal human urineBiochimica et Biophysica Acta (BBA) - General Subjects, 1972
- Genetic heterogeneity of α‐galactosidase in fabry's diseaseFEBS Letters, 1972
- Fabry's Disease: Differentiation between Two Forms of α-Galactosidase by MyoinositolScience, 1972
- Enzyme Replacement in Fabry's Disease, an Inborn Error of MetabolismScience, 1970
- Fabry's Disease: Alpha-Galactosidase DeficiencyScience, 1970
- Angiokeratoma corporis diffusum Fabry (Thesaurismosis hereditaria Ruiter-Pompen-Wyers)Dermatology, 1964
- Darstellung künstlicher Antigene mit determinanten Zuckergruppen, II. Mitteil.: Synthese der p ‐Aminophenyl‐ O ‐α‐glykoside von L ‐Fucose, L ‐Rhamnose, D ‐galaktose und D ‐MannoseEuropean Journal of Inorganic Chemistry, 1956