Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption

BACKGROUND: While role of ALDOB-related gene variants for hereditary fructose intolerance is well established, contribution of gene variants for acquired fructose malabsorption (e.g. SLC2A5, GLUT5) is not well understood. METHODS: Patients referred to fructose breath test were further selected to id...

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Detalles Bibliográficos
Autores principales: Taneva, Irina, Grumann, Dorothee, Schmidt, Dietmar, Taneva, Elina, von Arnim, Ulrike, Ansorge, Thomas, Wex, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985300/
https://www.ncbi.nlm.nih.gov/pubmed/35387598
http://dx.doi.org/10.1186/s12876-022-02244-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8985300/
https://www.ncbi.nlm.nih.gov/pubmed/35387598
http://dx.doi.org/10.1186/s12876-022-02244-7

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