Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome

<p dir="ltr">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 <i>SLC2A2</i> gene. <i>SLC2A2...

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المؤلف الرئيسي:	Sanaa Sharari (12561952) (author)
مؤلفون آخرون:	Basirudeen Kabeer (18295432) (author), Idris Mohammed (751020) (author), Basma Haris (12040355) (author), Igor Pavlovski (12561964) (author), Iman Hawari (12561958) (author), Ajaz Ahmad Bhat (12561955) (author), Mohammed Toufiq (7251596) (author), Sara Tomei (3441323) (author), Rebecca Mathew (6561392) (author), Najeeb Syed (12561967) (author), Sabah Nisar (12561961) (author), Selma Maacha (501715) (author), Jean-Charles Grivel (284645) (author), Damien Chaussabel (26369) (author), Johan Ericsson (49714) (author), Khalid Hussain (110443) (author)
منشور في:	2022
الموضوعات:	Biological sciences Genetics Biomedical and clinical sciences Clinical sciences Medical biochemistry and metabolomics Fanconi–Bickel syndrome (FBS) dysglycemia glucose transporter 2 (GLUT2) PBMCs (peripheral blood mononuclear cells) miRNAs
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Understanding the Role of GLUT2 in Dysglycemia Associated with Fanconi–Bickel Syndrome

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