The gliadin-CFTR connection: new perspectives for the treatment of celiac disease

Familial loss-of-function mutations of the gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) channel protein cause cystic fibrosis (CF), the most frequent inherited life-threatening disease in the Caucasian population. A recent study indicates that the gluten/gliadin-der...

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Detalles Bibliográficos
Autores principales: Maiuri, Luigi, Villella, Valeria R., Raia, Valeria, Kroemer, Guido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Commentary
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429699/
https://www.ncbi.nlm.nih.gov/pubmed/30898172
http://dx.doi.org/10.1186/s13052-019-0627-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6429699/
https://www.ncbi.nlm.nih.gov/pubmed/30898172
http://dx.doi.org/10.1186/s13052-019-0627-9

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