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...
I tiakina i:
| Ngā kaituhi matua: | , , , |
|---|---|
| Hōputu: | Artigo |
| Reo: | Inglês |
| I whakaputaina: |
BMC
2019-03-01
|
| Rangatū: | Italian Journal of Pediatrics |
| Ngā marau: | |
| Urunga tuihono: | http://link.springer.com/article/10.1186/s13052-019-0627-9 |
| Ngā Tūtohu: |
Kāore He Tūtohu, Me noho koe te mea tuatahi ki te tūtohu i tēnei pūkete!
|