Identification of ten novel SLC5A2 mutations and determination of the renal threshold for glucose excretion in Chinese patients with familial renal glucosuria
Author:
Publisher
Elsevier BV
Subject
Biochemistry, medical,Clinical Biochemistry,Biochemistry,General Medicine
Reference22 articles.
1. Determination of the renal threshold for glucose excretion in Familial Renal Glucosuria;Aires;Nephron,2015
2. A novel sodium–glucose co-transporter 2 gene (SGLT2) mutation contributes to the abnormal expression of SGLT2 in renal tissues in familial renal glucosuria;Yu;Int. Urol. Nephrol.,2014
3. Renal glucosuria;Brodehl;Pediatr. Nephrol. (Berlin, Germany),1987
4. Twenty-one additional cases of familial renal glucosuria: absence of genetic heterogeneity, high prevalence of private mutations and further evidence of volume depletion;Calado;Nephrol. Dial. Transplant.,2008
5. Familial renal glucosuria: SLC5A2 mutation analysis and evidence of salt-wasting;Calado;Kidney Int.,2006
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2. Performance of the ACMG‐AMP criteria in a large familial renal glucosuria cohort with identified SLC5A2 sequence variants;Clinical Genetics;2023-06-22
3. Mouse Models with SGLT2 Mutations: Toward Understanding the Role of SGLT2 beyond Glucose Reabsorption;International Journal of Molecular Sciences;2023-03-27
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