Clinical and genetic analysis in a patient with primary renal glucosuria: Identification of a novel mutation in the SLC5A2 gene

Primary renal glucosuria (PRG; OMIM #233100) is characterized by persistent glucosuria due to a reduction in the renal tubular reabsorption of glucose in the presence of a normal concentration of serum glucose and the absence of any other impairment of tubular function. The SLC5A2 gene is the causat...

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Detalles Bibliográficos
Autor principal: LEE, YONG-WHA
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829744/
https://www.ncbi.nlm.nih.gov/pubmed/24255686
http://dx.doi.org/10.3892/etm.2013.1326

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3829744/
https://www.ncbi.nlm.nih.gov/pubmed/24255686
http://dx.doi.org/10.3892/etm.2013.1326

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