Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

<div><p>Fanconi–Bickel Syndrome (FBS) is a rare disorder of carbohydrate metabolism that is characterized mainly by the accumulation of glycogen in the liver and kidney. It is inherited as an autosomal recessive disorder caused by mutations in the SLC2A2 gene, which encodes for GLUT2. Pa...

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المؤلف الرئيسي:	Sanaa Sharari (12561952) (author)
مؤلفون آخرون:	Mustapha Aouida (417652) (author), Idris Mohammed (751020) (author), Basma Haris (12040355) (author), Ajaz Ahmad Bhat (12561955) (author), Iman Hawari (12561958) (author), Sabah Nisar (12561961) (author), Igor Pavlovski (12561964) (author), Kabir H. Biswas (5705864) (author), Najeeb Syed (12561967) (author), Selma Maacha (501715) (author), Jean-Charles Grivel (284645) (author), Maryam Saifaldeen (12561970) (author), Johan Ericsson (49714) (author), Khalid Hussain (110443) (author)
منشور في:	2022
الموضوعات:	Biomedical and clinical sciences Clinical sciences Fanconi-Bickel syndrome (FBS) dysglycemia glucose transporter 2 (GLUT2) clustered regularly interspaced short palindromic repeats (CRISPR)- Cas9 sodium-glucose transport protein 2 (SGLT2)
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Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient

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