Clinical and genetic analysis in a patient with primary renal glucosuria: Identification of a novel mutation in the SLC5A2 gene

Podobne knjige/članki

• Novel SLC5A2 mutation contributes to familial renal glucosuria: Abnormal expression in renal tissues
  od: Yu, Lei, et al.
  Izdano: (2016)
• SLC5A2 mutations, including two novel mutations, responsible for renal glucosuria in Chinese families
  od: Yu, Lei, et al.
  Izdano: (2020)
• A novel compound heterozygous mutation in SLC5A2 contributes to familial renal glucosuria in a Chinese family, and a review of the relevant literature
  od: Li, Shentang, et al.
  Izdano: (2019)
• Acquired renal glucosuria in an undifferentiated connective tissue disease patient with a SLC5A2 heterozygous mutation: A case report
  od: Gu, Xiangchen, et al.
  Izdano: (2018)
• A recurrent deletion in the SLC5A2 gene including the intron 7 branch site responsible for familial renal glucosuria
  od: Zhao, Xiangzhong, et al.
  Izdano: (2016)