GENETIC STUDIES IN GLYCOGEN STORAGE DISEASE TYPE III
- 1 September 1970
- journal article
- Published by Wiley in Acta Paediatrica
- Vol. 59 (5) , 529-535
- https://doi.org/10.1111/j.1651-2227.1970.tb16803.x
Abstract
No abstract availableKeywords
This publication has 11 references indexed in Scilit:
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- 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
- Hepatic Phosphorylase DefectAmerican Journal of Diseases of Children, 1966
- GLYCOGEN STORAGE DISEASEActa Pathologica Microbiologica Scandinavica, 1965
- Glycogen Storage Diseases, Types III, IV, and VIPublished by Wiley ,1964
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- Amylo-1,6-glucosidase activity in leucocytes from patients with glycogen storage diseaseClinica Chimica Acta; International Journal of Clinical Chemistry, 1963
- LEUKOCYTE DEBRANCHING ENZYME IN GLYCOGEN STORAGE DISEASEJournal of Clinical Investigation, 1963