MOLECULAR AND FUNCTIONAL BASIS OF THE TYPE 1 GLYCOGEN STORAGE DISEASE SUBTYPES DUE TO THE DEFICIENCY OF TRANSPORT PROTEIN COMPONENTS OF THE LIVER GLUCOSE-6-PHOSPHATASE SYSTEMS
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Glucose 6-phosphate transport in fibroblast microsomes from glycogen storage disease type 1b patients:: evidence for multiple glucose 6-phosphate transport systems
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Histone 2A stimulates glucose-6-phosphatase activity by permeabilization of liver microsomes
- JOURNAL OF BIOLOGICAL CHEMISTRY
Conformational change of the catalytic subunit of glucose-6-phosphatase in rat liver during the fetal-to-neonatal transition
