Fanconi–Bickel syndrome – A congenital defect of the liver‐type facilitative glucose transporter
- 1 June 1998
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 21 (3) , 191-194
- https://doi.org/10.1023/a:1005379013406
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Mutations in GLUT2, the gene for the liver-type glucose transporter, in patients with Fanconi-Bickel syndromeNature Genetics, 1997
- The GLUT5 hexose transporter is also localized to the basolateral membrane of the human jejunumBiochemical Journal, 1995
- Rapid reversible substrate regulation of fructose transporter expression in rat small intestine and kidneyAmerican Journal of Physiology-Gastrointestinal and Liver Physiology, 1994
- Fanconi-Bickel syndromePediatric Nephrology, 1987
- [Chronic aminoaciduria (amino acid diabetes or nephrotic-glucosuric dwarfism) in glycogen storage and cystine disease].1949