Combined features of low phospholipid-associated cholelithiasis and progressive familial intrahepatic cholestasis 3
Author:
Publisher
Wiley
Subject
Hepatology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1478-3231.2009.02148.x/fullpdf
Reference13 articles.
1. 1.â Jacquemin E , de Vree JM , Cresteil D , et al. The wide spectrum of multidrug resistance 3 deficiency: from neonatal cholestasis to cirrhosis of adulthood. Gastroenterology 2001; 120: 1448â58.
2. 2.â Degiorgio D , Colombo C , Seia M , et al. Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3). Eur J Hum Genet 2007; 15: 1230â8.
3. 3.â Keitel V , Burdelski M , Warskulat U , et al. Expression and localization of hepatobiliary transport proteins in progressive familial intrahepatic cholestasis. Hepatology 2005; 41: 1160â72.
4. 4.â Rosmorduc O , Hermelin B , Poupon R. MDR3 gene defect in adults with symptomatic intrahepatic and gallbladder cholesterol cholelithiasis. Gastroenterology 2001; 120: 1459â67.
5. 5.â Rosmorduc O , Hermelin B , Boelle PY , et al. ABCB4 gene mutation-associated cholelithiasis in adults. Gastroenterology 2003; 125: 452â9.
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5. Combined Mutations of Canalicular Transporter Proteins Causing Low Phospholipid-Associated Cholelithiasis and Transient Neonatal Cholestasis in an Infant;JPGN Reports;2021-04-22
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