Sodium‐glucose cotransporter type 2 channel inhibitor: Breakthrough in the treatment of neutropenia in patients with glycogen storage disease type 1b?

Glycogen storage disease type 1b (GSD 1b) is an inherited metabolic defect caused by biallelic mutations in the SLC37A4 gene encoding microsomal glucose‐6‐phosphate (G6P) transporter in the endoplasmic reticulum (ER) membrane. Ineffective G6P transport into the ER leads to hypoglycaemia, hyperlactat...

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Detalles Bibliográficos
Autores principales: Kaczor, Magdalena, Greczan, Milena, Kierus, Karolina, Ehmke vel Emczyńska‐Seliga, Ewa, Ciara, Elżbieta, Piątosa, Barbara, Rokicki, Dariusz, Książyk, Janusz, Wesół‐Kucharska, Dorota
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons, Inc. 2022
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995836/
https://www.ncbi.nlm.nih.gov/pubmed/35433171
http://dx.doi.org/10.1002/jmd2.12278

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8995836/
https://www.ncbi.nlm.nih.gov/pubmed/35433171
http://dx.doi.org/10.1002/jmd2.12278

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