The gliadin-CFTR connection: new perspectives for the treatment of celiac disease
Abstract 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/gl...
Tallennettuna:
| Päätekijät: | , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
BMC
2019-03-01
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| Sarja: | Italian Journal of Pediatrics |
| Aiheet: | |
| Linkit: | http://link.springer.com/article/10.1186/s13052-019-0627-9 |
| Tagit: |
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