Genetic Loss of Sucrase-Isomaltase Function: Mechanisms, Implications, and Future Perspectives

Genetic variants causing loss of sucrase-isomaltase (SI) function result in malabsorption of sucrose and starch components and the condition congenital sucrase-isomaltase deficiency (CSID). The identified genetic variants causing CSID are very rare in all surveyed populations around the globe, excep...

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Detalles Bibliográficos
Autores principales: Senftleber, Ninna Karsbæk, Ramne, Stina, Moltke, Ida, Jørgensen, Marit Eika, Albrechtsen, Anders, Hansen, Torben, Andersen, Mette K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041990/
https://www.ncbi.nlm.nih.gov/pubmed/36994449
http://dx.doi.org/10.2147/TACG.S401712

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10041990/
https://www.ncbi.nlm.nih.gov/pubmed/36994449
http://dx.doi.org/10.2147/TACG.S401712

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