Gene variants of the SLC2A5 gene encoding GLUT5, the major fructose transporter, do not contribute to clinical presentation of acquired fructose malabsorption
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DOI: 10.1186/s12876-022-02244-7
Abstract: 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… read more here.
Keywords: fructose malabsorption; gene variants; slc2a5 gene; gene ... See more keywords