Fabry's disease: evidence for a physically altered -galactosidase.

References

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Fabry's Disease: Classification as a Sphingolipidosis and Partial Characterization of a Novel Glycolipid Charles C. Sweeley, Bernard Klionsky Journal of Biological Chemistry Partial CharacterizationPathologyMedicineNovel GlycolipidLysosomal Storage Disease	1963	398
Gaucher's Disease: Deficiency of “cid”β-Glucosidase and Reconstitution of Enzyme Activity <i>In Vitro</i> Mae Wan Ho, John S. O’Brien Proceedings of the National Academy of Sciences Factor PAutoimmune DiseaseBiochemistryPathogenesisGlycobiology	1971	259
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Adult Gaucher's disease: kindred studies and demonstration of a deficiency of acid beta-glucosidase in cultured fibroblasts. M. W. Ho, J. Seck, David J. Schmidt, PubMed Acid Beta-glucosidaseInherited Metabolic DiseaseGlycobiologyCultured FibroblastsPathology	1972	91

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