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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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Библиографические подробности
Опубликовано в: :BMC Nephrol
Главные авторы: Yu, Lei, Wu, Meng, Hou, Ping, Zhang, Hong
Формат: Artigo
Язык:Inglês
Опубликовано: BioMed Central 2020
Предметы:
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC7047355/
https://ncbi.nlm.nih.gov/pubmed/32111189
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12882-020-01725-9
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