Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues

Documenti analoghi

• SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families
  di: Yu, Lei, et al.
  Pubblicazione: (2020)
• A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature
  di: Li, Shentang, et al.
  Pubblicazione: (2019)
• Clinical and genetic analysis in a patient with primary renal glucosuria: Identification of a novel mutation in the SLC5A2 gene
  di: LEE, YONG-WHA
  Pubblicazione: (2013)
• Acquired renal glucosuria in an undifferentiated connective tissue disease patient with a SLC5A2 heterozygous mutation: A case report
  di: Gu, Xiangchen, et al.
  Pubblicazione: (2018)
• Hypouricaemia and hyperuricosuria in familial renal glucosuria
  di: Aires, Inês, et al.
  Pubblicazione: (2013)