SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families

BACKGROUND: Familial renal glucosuria (FRG) is characterized by persistent glucosuria without other impairments of tubular function in the presence of normal serum glucose. SGLT2, which is almost exclusively expressed in the kidney, accounts for most of the glucose reabsorption. Recently, some studi...

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Detalles Bibliográficos
Autores principales: Yu, Lei, Wu, Meng, Hou, Ping, Zhang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047355/
https://www.ncbi.nlm.nih.gov/pubmed/32111189
http://dx.doi.org/10.1186/s12882-020-01725-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7047355/
https://www.ncbi.nlm.nih.gov/pubmed/32111189
http://dx.doi.org/10.1186/s12882-020-01725-9

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