Studies in Glycogen Storage Disease Type III: Kinetics of Amylo-1,6-Glucosidase in Human Erythrocytes
- 1 January 1971
- journal article
- research article
- Published by Taylor & Francis in Scandinavian Journal of Clinical and Laboratory Investigation
- Vol. 27 (3) , 269-272
- https://doi.org/10.3109/00365517109080218
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
- GENETIC STUDIES IN GLYCOGEN STORAGE DISEASE TYPE IIIActa Paediatrica, 1970
- Glyogen-storage disease type VIa: Low phosphorylase kinase activity caused by a low enzyme-substrate affinityBiochimica et Biophysica Acta (BBA) - Enzymology, 1970
- A rapid micro assay method for amylo-1,6-glucosidaseAnalytical Biochemistry, 1970
- Purification and properties of rabbit muscle amylo-1,6-glucosidase-oligo-1,4 →1,4-transferaseBiochemistry, 1969
- Muscle Phosphofructokinase DeficiencyArchives of Neurology, 1967
- The Subgroups of Type III GlycogenosisEuropean Journal of Biochemistry, 1967
- The Determination of Amylo-1,6-GlucosidaseEuropean Journal of Biochemistry, 1967
- Amylo-1,6-Glucosidase Activity and Glycogen Content of the Erythrocytes of Normal Subjects, Patients with Glycogen Storage Disease and HeterozygotesEuropean Journal of Biochemistry, 1967
- Allotypy and EniotypyNature, 1966
- Studies on amylo-1,6-glucosidaseBiochimica et Biophysica Acta, 1956