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    Dimitrios T. Papadimitriou et al, 2021, Journal of Diabetes CrossRef
  2. NovelSLC5A2Variants Contribute to Renal Glucosuria in Chinese Families: Abnormal Expression and Dysfunction of Variant SLC5A2
    Lei Yu et al, 2015, Human Mutation CrossRef
  3. Novel SLC5A2 Mutations and Genetic Characterization in Korean Patients with Familial Renal Glucosuria
    Weon Kyung Lee et al, 2018, Childhood Kidney Diseases CrossRef
  4. Hereditary tubulopathies accompanying polyuia
    M. O. Ryznychuk et al, 2021, Regulatory Mechanisms in Biosystems CrossRef
  5. Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues
    Lei Yu et al, 2016, Experimental and Therapeutic Medicine CrossRef
  6. A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria
    Xiangzhong Zhao et al, 2016, Scientific Reports CrossRef
  7. A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature
    Shentang Li et al, 2019, Molecular Medicine Reports CrossRef
  8. De Novo Expression of Sodium-Glucose Cotransporter SGLT2 in Bowman’s Capsule Coincides with Replacement of Parietal Epithelial Cell Layer with Proximal Tubule-like Epithelium
    Niloofar M. Tabatabai et al, 2014, The Journal of Membrane Biology CrossRef