SLC5A1 Variants in Turkish Patients with Congenital Glucose-Galactose Malabsorption

Congenital glucose-galactose malabsorption is a rare autosomal recessive disorder caused by mutations in SLC5A1 encoding the apical sodium/glucose cotransporter SGLT1. We present clinical and molecular data from eleven affected individuals with congenital glucose-galactose malabsorption from four un...

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Detalles Bibliográficos
Autores principales: Hoşnut, Ferda Ö., Janecke, Andreas R., Şahin, Gülseren, Vogel, Georg F., Lafcı, Naz G., Bichler, Paul, Müller, Thomas, Huber, Lukas A., Valovka, Taras, Aksu, Aysel Ü.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379334/
https://www.ncbi.nlm.nih.gov/pubmed/37510265
http://dx.doi.org/10.3390/genes14071359

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10379334/
https://www.ncbi.nlm.nih.gov/pubmed/37510265
http://dx.doi.org/10.3390/genes14071359

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