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Items: 4

1.
SLC10A2 deficiency‐induced congenital chronic bile acid diarrhea and stunting
Di Qie, Yulin Zhang, Xue Gong, Yunru He, Lina Qiao, Guoyan Lu, Yifei Li
Mol Genet Genomic Med. 2021 Aug; 9(8): e1740. Published online 2021 Jun 30. doi: 10.1002/mgg3.1740
PMCID:
PMC8404231
AbstractArticlePDF–755K
2.
A Variant of the SLC10A2 Gene Encoding the Apical Sodium-Dependent Bile Acid Transporter Is a Risk Factor for Gallstone Disease
Olga Renner, Simone Harsch, Elke Schaeffeler, Stefan Winter, Matthias Schwab, Marcin Krawczyk, Jonas Rosendahl, Henning Wittenburg, Frank Lammert, Eduard F. Stange
PLoS One. 2009; 4(10): e7321. Published online 2009 Oct 13. doi: 10.1371/journal.pone.0007321
PMCID:
PMC2757911
AbstractArticlePDF–112K
3.
Primary bile acid malabsorption caused by mutations in the ileal sodium-dependent bile acid transporter gene (SLC10A2).
P Oelkers, L C Kirby, J E Heubi, P A Dawson
J Clin Invest. 1997 Apr 15; 99(8): 1880–1887. doi: 10.1172/JCI119355
PMCID:
PMC508012
SummaryPDF–420K
4.
Point mutations in the ileal bile salt transporter cause leaks in the enterohepatic circulation leading to severe chronic diarrhea and malabsorption.
D M Small
J Clin Invest. 1997 Apr 15; 99(8): 1807–1808. doi: 10.1172/JCI119345
PMCID:
PMC508002
SummaryPDF–84K

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