Coinheritance of Gilbert syndrome–associatedUGT1A1 mutation increases gallstone risk in cystic fibrosis
Author:
Publisher
Wiley
Subject
Hepatology
Reference23 articles.
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2. , , , , . Cystic fibrosis transmembrane conductance regulator gene mutations cause “black” pigment gallstone formation: new insights from mouse models and implications for therapeutic interventions in cystic fibrosis. In: , , , eds. Gallstone Pathogenesis and Treatment. Lancaster: Kluwer Academic Publishers, 2004: 24–27.
3. Gallstones in cystic fibrosis: A critical reappraisal
4. Failure of ursodeoxycholic acid to dissolve radiolucent gallstones in patients with cystic fibrosis
5. Enterohepatic cycling of bilirubin: A putative mechanism for pigment gallstone formation in ileal Crohn's disease☆, ☆☆
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