Simultaneous absence of α-1,4-glucosidase and α-1,6-glucosidase activities (pH 4) in tissues of children with Type II glycogen storage disease
- 1 March 1970
- journal article
- research article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 9 (6) , 1423-1428
- https://doi.org/10.1021/bi00808a017
Abstract
No abstract availableThis publication has 10 references indexed in Scilit:
- Lysosomal α-glucosidase. I. Purification and properties of the rat liver enzymeBiochemistry, 1970
- Lysosomal α-glucosidase. II. Kinetics of action of the rat liver enzymeBiochemistry, 1970
- Further purification and characterization of the acid α-glucosidaseBiochemical Journal, 1968
- Glycogen-Storage Diseases**This review is dedicated to Carl F. Cori on the occasion of his seventieth birthday.: Types I, III, IV, V, VII and Unclassified GlycogenosesPublished by Elsevier ,1968
- Purification of an acid α-glucosidase by dextran-gel filtrationBiochemical Journal, 1967
- α-1,4-Glucosidase Activity in Leucocytes from the Family of Two Brothers Who Lack this Enzyme in MuscleBiochemical Journal, 1966
- Cardiac glycogenosisThe Journal of Pediatrics, 1966
- The subcellular distribution of enzymes in type II glycogenosis and the occurrence of an oligo-α-1,4-glucan glucohydrolase in human tissuesBiochimica et Biophysica Acta (BBA) - Enzymology and Biological Oxidation, 1965
- α-Glucosidase deficiency in generalized glycogen-storage disease (Pompe's disease)Biochemical Journal, 1963
- Tissue fractionation studies. 16. Intracellular distribution and properties of α-glucosidases in rat liverBiochemical Journal, 1963