Galactosylgalactosylglucosylceramide: Galactosyl hydrolase in normal human plasma and its absence in patients with fabry's disease
Author:
Publisher
Wiley
Subject
Cell Biology,Genetics,Molecular Biology,Biochemistry,Structural Biology,Biophysics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1016/0014-5793(70)80151-X/fullpdf
Reference12 articles.
1. Enzymatic Defect in Fabry's Disease
2. Fabry's Disease: Classification as a Sphingolipidosis and Partial Characterization of a Novel Glycolipid
3. A BIOCHEMICAL INVESTIGATION OF ANGIOKERATOMA CORPORIS DIFFUSUM
4. Concentrations of glycosyl ceramides in plasma and red cells in Fabry's disease, a glycolipid lipidosis
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1. Prenatal Diagnosis of Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;2010-09-24
2. Disorders of Lipid Metabolism;Genetic Disorders and the Fetus;1986
3. Differential assay for lysosomal alpha-galactosidases in human tissues and its application to Fabry's disease;Clinica Chimica Acta;1981-05
4. Enzyme therapy in Fabry disease: differential in vivo plasma clearance and metabolic effectiveness of plasma and splenic alpha-galactosidase A isozymes.;Proceedings of the National Academy of Sciences;1979-10-01
5. Factors affecting the hydrolysis of ceramide-3 by α-galactosidase a from human liver;Biochimica et Biophysica Acta (BBA) - Enzymology;1979-05
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