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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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| Publicat a: | Ital J Pediatr |
|---|---|
| Autors principals: | , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
BioMed Central
2019
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6429699/ https://ncbi.nlm.nih.gov/pubmed/30898172 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13052-019-0627-9 |
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