Yüklüyor......
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...
Kaydedildi:
| Yayımlandı: | Ital J Pediatr |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
BioMed Central
2019
|
| Konular: | |
| Online Erişim: | 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 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|