Associated Papers
A BCB4 variant is associated with hepatobiliary MR abnormalities in people with low-phospholipid-associated cholelithiasis syndrome.
Biyoukar M et al.
Jhep Reports : Innovation in Hepatology, 2022
36277956 (PubMed )
Supplement: mmc1.pdf
Genetics in Familial Intrahepatic Cholestasis: Clinical Patterns and Development of Liver and Biliary Cancers: A Review of the Literature.
Vitale G et al.
Cancers, 2022
A homozygous ABCB4 mutation causing an LPAC syndrome evolves into cholangiocarcinoma.
Khabou B et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2019
Select a paper to view details