Type Ib glycogen storage disease is caused by a defect in the glucose-6-phosphate translocase of the microsomal glucose-6-phosphatase system.
Open Access
- 1 September 1980
- journal article
- research article
- Published by Elsevier in Journal of Biological Chemistry
- Vol. 255 (18) , 8381-8384
- https://doi.org/10.1016/s0021-9258(18)43502-8
Abstract
No abstract availableThis publication has 16 references indexed in Scilit:
- A new variant of glycogen storage disease Type I probably due to a defect in the glucose-6-phosphate transport systemBiochemical and Biophysical Research Communications, 1978
- A modification of the Lowry procedure to simplify protein determination in membrane and lipoprotein samplesAnalytical Biochemistry, 1978
- Evidence for the Involvement of a Glucose‐6‐Phosphate Carrier in Microsomal Glucose‐6‐Phosphatase ActivityEuropean Journal of Biochemistry, 1978
- Microsomal membrane permeability and the hepatic glucose-6-phosphatase system. Interactions of the system with D-mannose 6-phosphate and D-mannose.Journal of Biological Chemistry, 1976
- On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphataseMolecular and Cellular Biochemistry, 1975
- Kinetics of the Glucose 6-Phosphate-Glucose Exchange Activity and Glucose Inhibition of Glucose 6-Phosphatase of Intact and Disrupted Rat Liver MicrosomesJournal of Biological Chemistry, 1973
- Studies of Liver Glycogenoses, with Particular Reference to the Metabolism of Intravenously Administered GlycerolNew England Journal of Medicine, 1968
- [111] Glucose-6-phosphatasePublished by Elsevier ,1966
- PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTJournal of Biological Chemistry, 1951
- The Determination of Enzyme Dissociation ConstantsJournal of the American Chemical Society, 1934