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A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature

Familial renal glucosuria (FRG) is a rare condition that involves isolated glucosuria despite normal blood glucose levels. Mutations in the solute carrier family 5 member 2 (SLC5A2) gene, which encodes sodium-glucose cotransporter 2 (SGLT2), have been reported to be responsible for the disease. Gene...

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Detalles Bibliográficos
Autores principales:	Li, Shentang, Yang, Yeyi, Huang, Lihua, Kong, Min, Yang, Zuocheng
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	D.A. Spandidos 2019
Materias:	Articles
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6472135/ https://www.ncbi.nlm.nih.gov/pubmed/30942416 http://dx.doi.org/10.3892/mmr.2019.10110

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