Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors
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DOI: 10.3390/diagnostics13101803
Abstract: Glycogen storage disease type Ib (GSD1b) is due to a defect in the glucose-6-phosphate transporter (G6PT) of the endoplasmic reticulum, which is encoded by the SLC37A4 gene. This transporter allows the glucose-6-phosphate that is made… read more here.
Keywords: gsd1b; g6pc3 deficiency; treatment; neutropenia associated ... See more keywords