Загрузка...
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...
Сохранить в:
| Опубликовано в: : | BMC Nephrol |
|---|---|
| Главные авторы: | , , , |
| 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 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|