Associated Papers
Fanconi-Bickel Syndrome: A Review of the Mechanisms That Lead to Dysglycaemia.
Sharari S et al.
International Journal of Molecular Sciences, 2020
Functional and structural analysis of rare SLC2A2 variants associated with Fanconi-Bickel syndrome and metabolic traits.
Enogieru OJ et al.
Human Mutation, 2019
Mutation analysis of the GLUT2 gene in three unrelated Egyptian families with Fanconi-Bickel syndrome: revisited gene atlas for renumbering.
Al-Haggar M et al.
Clinical and Experimental Nephrology, 2012
Fanconi-Bickel syndrome as an example of marked allelic heterogeneity.
Al-Haggar M
World Journal of Nephrology, 2012
Fanconi Bickel Syndrome: Novel Mutations in GLUT 2 Gene Causing a Distinguished Form of Renal Tubular Acidosis in Two Unrelated Egyptian Families.
Al-Haggar M et al.
Case Reports in Nephrology, 2011
The mutation spectrum of the facilitative glucose transporter gene SLC2A2 (GLUT2) in patients with Fanconi-Bickel syndrome.
Santer R et al.
Human Genetics, 2002
Mutation analysis of the GLUT2 gene in patients with Fanconi-Bickel syndrome.
Sakamoto O et al.
Pediatric Research, 2000
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