Article

Understanding the role of GLUT2 in dysglycemia associated with Fanconi-Bickel syndrome

2022-03-18

Abstract excerpt

Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized by the accumulation of glycogen mainly in the liver. It is inherited in an autosomal recessive manner due to mutations in the SLC2A2 gene. SLC2A2 encodes for the glucose transporter GLUT2 and is expressed in tissues that are involved in glucose homeostasis. The molecular mechanisms of dysglycemia in FBS are still not...

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Literature Corpus work: 90d97f02-06e6-5f4d-907f-3583c63d4392
DOI: 10.21203/rs.3.rs-1401570/v1

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