Associated Papers
Single nucleotide variants of the SLC2A2 gene in Mexican-origin population.
Gutiérrez-García CA et al.
Gaceta Medica De Mexico, 2025
Genetic variant profiling of neonatal diabetes mellitus in Iranian patients: Unveiling 58 distinct variants in 14 genes.
Mianesaz H et al.
Journal of Diabetes Investigation, 2024
Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.
Sharari S et al.
International Journal of Molecular Sciences, 2020
Segregation of a novel homozygous 6 nucleotide deletion in GLUT2 gene in a Fanconi-Bickel syndrome family.
Abbasi F et al.
Gene, 2015
SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion.
Sansbury FH et al.
Diabetologia, 2012
Select a paper to view details