Associated Papers
Molecular Epidemiology of Na+-Taurocholate Cotransporting Polypeptide Deficiency in Guangdong Province, China: A Pilot Study by Screening for Four Prevalent Variants of the Causative Gene SLC10A1.
Li H et al.
Frontiers in Genetics, 2022
Whole-exome sequencing expands the roles of novel mutations of organic anion transporting polypeptide, ATP-binding cassette transporter, and receptor genes in intrahepatic cholestasis of pregnancy.
Liu X et al.
Frontiers in Genetics, 2022
36046230 (PubMed )
Supplement: Table3.XLSX › Sheet1
Homozygous p.Ser267Phe in SLC10A1 is associated with a new type of hypercholanemia and implications for personalized medicine.
Liu R et al.
Scientific Reports, 2017
28835676 (PubMed )
Supplement: 41598_2017_7012_MOESM1_ESM.doc
A genetic variant of the NTCP gene is associated with HBV infection status in a Chinese population.
Yang J et al.
Bmc Cancer, 2016
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