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Treatment of the Neutropenia Associated with GSD1b and G6PC3 Deficiency with SGLT2 Inhibitors

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 in the cytosol to cross the endoplasmic reticulum (ER) membrane a...

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Detalles Bibliográficos
Autores principales:	Veiga-da-Cunha, Maria, Wortmann, Saskia B., Grünert, Sarah C., Van Schaftingen, Emile
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	MDPI 2023
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10217388/ https://www.ncbi.nlm.nih.gov/pubmed/37238286 http://dx.doi.org/10.3390/diagnostics13101803

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