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Understanding the Mechanism of Dysglycemia in a Fanconi-Bickel Syndrome Patient
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. Patients with FBS have...
Autores principales: | Sharari, Sanaa, Aouida, Mustapha, Mohammed, Idris, Haris, Basma, Bhat, Ajaz Ahmad, Hawari, Iman, Nisar, Sabah, Pavlovski, Igor, Biswas, Kabir H., Syed, Najeeb, Maacha, Selma, Grivel, Jean-Charles, Saifaldeen, Maryam, Ericsson, Johan, Hussain, Khalid |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9159359/ https://www.ncbi.nlm.nih.gov/pubmed/35663312 http://dx.doi.org/10.3389/fendo.2022.841788 |
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