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Scandinavian Journal of Clinical and Laboratory Investigation Volume 27, 1971 - Issue 3
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Original Article

Studies in Glycogen Storage Disease Type III: Kinetics of Amylo-1,6-Glucosidase in Human Erythrocytes

Else Garatun-Tjeldstö Dept. of Biochemistry, University of Bergen, Bergen, Norway
&
O. Garatun-Tjeldstö Dept. of Biochemistry, University of Bergen, Bergen, Norway
Pages 269-272 | Received 28 Sep 1970, Accepted 28 Dec 1970, Published online: 08 Jul 2009

References

  • Brown D. H., Illingworth B. The role of oligo-1,4 $ 1,4-glucantransferase and amylo-1,6-glucosidase in the debranching of glycogen. Control of Glycogen Metabolism, Ciba Foundation Symposium, W. J. Whelan, M. P. Cameron. J. & A. Churchill Ltd., London 1964; 139–150
  • Chayoth R., Moses S. W., Steinitz K. Debrancher enzyme activity in the blood cells of families with type III glycogen storage disease. Israel J. med. Sci. 1967; 3: 422
  • Cinader B., Dubiski S., Wardlaw A. C. Allotypy and eniotypy. Nature 1966; 210: 1291
  • Hers H. G., Verhue W., Van Hoof F. The determination of amylo-1,6-glucosidase. Europ. J. Biochem. 1967; 2: 257
  • Huijing F. Glycogen storage disease VIa: Low phosphorylase kinase activity caused by a low enzyme-substrate affinity. Biochim. biophys. Acta. (Amst.) 1970; 206: 199
  • Larner J., Shliselfeld L. H. Studies on Amylo-1,6-glucosidase. Biochim. biophys. Acta. (Amst.) 1956; 20: 53
  • Layzer R. B., Rowland L. P., Ranney H. M. Muscle phosphofructokinase deficiency. Arch. Neurol. (Chic.) 1967; 17: 512
  • Levin S., Moses S. W., Chayoth R., Jagoda N., Steinitz K. Glycogen storage disease in Israel. A clinical, biochemical and genetic study. Israel J. med. Sci. 1967; 3: 397
  • Mahler R. Glycogen storage diseases and galactosaemia. Biochemical Disorders in Human Disease. 3rd ed., R. H. S. Thompson, I. D. Wootton. J. & A. Churchill Ltd., London 1970; 95–127
  • Nelson T. E., Kolb E., Larner J. Purification and properties of rabbit muscle amylo-1,6-glucosidase-oligo-1,4 $ 1,4-transferase. Biochemistry. 1969; 8: 1419
  • Nelson T. E., Larner J. A rapid micro assay method for amylo-1,6-glucosidase. Analyt. Biochem. 1970; 33: 87
  • Taylor P. M., Whelan W. J. (1968) Rabbit muscle amylo-1,6-glucosidase: Properties and evidence of heterogeneity. Control of Glycogen Metabolism. FEBS Proceedings of the Fourth Meeting in Oslo Universitetsforlaget, Oslo, July, 3–71967, W. J. Whelan. Academic Press, London & New York, 101–114
  • Van Hoof F. Amylo-1,6-glucosidase activity and glycogen content of the erythrocytes of normal subjects, patients with glycogen storage disease and heterozygotes. Europ. J. Biochem. 1967; 2: 271
  • Van Hoof F., Hers H. G. The subgroups of type III glycogenosis. Europ. J. Biochem. 1967; 2: 265
  • Waaler P. E., Garatun-Tjeldstö O., Moe P. J. Genetic studies in glycogen storage disease type III. Acta. paediat. scand. 1970; 59: 529

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