1. Relevance of solute carrier family 5 transporter defects to inherited and acquired human disease
   Miryam Cannizzaro et al, 2019, Journal of Applied Genetics CrossRef
2. Case report: Identification of three novel compound heterozygous SGLT2 variants in three Chinese pediatric patients with familial renal glucosuria
   Huimei Huang et al, 2022, Frontiers in Pediatrics CrossRef