- Presentation of Progressive Familial Intrahepatic Cholestasis Type 3 Mimicking Wilson Disease: Molecular Genetic Diagnosis and Response to Treatment
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Boga S, Jain D, Schilsky M
- KMID: 2068799
- Pediatr Gastroenterol Hepatol Nutr.
- 2015 Sep;18(3):202-208.
- doi: 10.5223/pghn.2015.18.3.202
Progressive familial intrahepatic cholestasis type 3 (PFIC3) is an autosomal recessive disorder of cholestasis of hepatocellular origin, typically seen in infancy or childhood caused by a defect in the ABCB4... -
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