Clinical and genetic analysis in a family with familial renal glucosuria: Identification of an N101K mutation in the sodium–glucose cotransporter 2 encoded by a solute carrier family 5 member 2 gene

We report the identification of a mutation in the solute carrier family 5 member 2 (SLC5A2) gene, which encodes sodium–glucose cotransporter 2, in a family with familial renal glucosuria. The proband was a 26‐year‐old Japanese man referred to the diabetes division with repeated glucosuria without hy...

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Detalles Bibliográficos
Autores principales: Sada, Kentaro, Hidaka, Shuji, Imaishi, Nao, Shibata, Kohei, Katashima, Rumi, Noso, Shinsuke, Ikegami, Hiroshi, Kakuma, Tetsuya, Shibata, Hirotaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232273/
https://www.ncbi.nlm.nih.gov/pubmed/31584752
http://dx.doi.org/10.1111/jdi.13157

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7232273/
https://www.ncbi.nlm.nih.gov/pubmed/31584752
http://dx.doi.org/10.1111/jdi.13157

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