[Such an impairment could be due to genetic factors, like mutations of the anion exchanger 2 (a variant of the Cl⁻/HCO₃⁻ exchanger) in primary biliary cirrhosis or of TGR5 (a bile salt receptor implicated in the regulation of HCO₃⁻ secretion) in primary sclerosing cholangitis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
Gene-disease associations inferred from text-mining the literature.
DisGeNET evidence - LITERATURE