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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

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