A direct evidence for defect in glucose-6-phosphate transport system in hepatic microsomal membrane of glycogen storage disease type Ib
- 1 March 1984
- journal article
- research article
- Published by Elsevier in Biochemical and Biophysical Research Communications
- Vol. 119 (2), 593-597
- https://doi.org/10.1016/s0006-291x(84)80290-9
Abstract
No abstract availableThis publication has 13 references indexed in Scilit:
- Glycogen Storage Disease Type 1b: Microsomal Glucose-6-Phosphatase System in Two Patients with Different Clinical FindingsPediatric Research, 1983
- Glycogen storage disease type 1b due to a defect of glucose‐6‐phosphate translocaseJournal of Inherited Metabolic Disease, 1982
- Glycogenosis type Ib. Further evidence for a membrane diseaseEuropean Journal of Pediatrics, 1981
- Neutropenia and impaired neutrophil migration in type IB glycogen storage diseaseThe Journal of Pediatrics, 1980
- A new variant of glycogen storage disease type 1: Probably due to a defect in the glucose‐6‐phosphate transport systemJournal of Inherited Metabolic Disease, 1979
- 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
- On the involvement of a glucose 6-phosphate transport system in the function of microsomal glucose 6-phosphataseMolecular and Cellular Biochemistry, 1975
- A simple procedure for the isolation of rat liver microsomesFEBS Letters, 1971