Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues

Familial renal glucosuria (FRG) is characterized by persistent glucosuria in the presence of normal serum glucose concentrations, while other impairments of tubular function are absent. Mutations in the sodium-glucose co-transporter 2 (SLC5A2) gene have been found to be responsible for FRG. However,...

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Detalles Bibliográficos
Autores principales: Yu, Lei, Hou, Ping, Liu, Guo-Ping, Zhang, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2016
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950299/
https://www.ncbi.nlm.nih.gov/pubmed/27446256
http://dx.doi.org/10.3892/etm.2016.3388

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4950299/
https://www.ncbi.nlm.nih.gov/pubmed/27446256
http://dx.doi.org/10.3892/etm.2016.3388

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