Hepatic steatosis in Wilson disease - Role of copper and PNPLA3 mutations

Journal of Hepatology

Volumn 63, Issue 1, 2015, Pages 156-163

  Stättermayer, Albert Friedrich ^a   Traussnigg, Stefan ^a   Dienes, Hans Peter ^a   Aigner, Elmar ^b   Stauber, Rudolf ^c   Lackner, Karoline ^c   Hofer, Harald ^a   Stift, Judith ^a   Wrba, Friedrich ^a   Stadlmayr, Andreas ^d   Datz, Christian ^d   Strasser, Michael ^b   Maieron, Andreas ^e   Trauner, Michael ^a   Ferenci, Peter ^a  

^a MEDICAL UNIVERSITY OF VIENNA   (Austria)

^b PARACELSUS MEDICAL UNIVERSITY   (Austria)

^c MEDICAL UNIVERSITY OF GRAZ   (Austria)

^d Department of General Surgery   (Austria)

^e KH der Elisabethinen   (Austria)

Author keywords

ATP7B; Copper; PNPLA3; Steatohepatitis; Steatosis; Wilson disease

Indexed keywords

COPPER; PATATIN LIKE PHOSPHOLIPASE DOMAIN CONTAINING 3; PROTEIN; UNCLASSIFIED DRUG; ADIPONUTRIN, HUMAN; DNA; MEMBRANE PROTEIN; TRIACYLGLYCEROL LIPASE;

ADOLESCENT; ADULT; ARTICLE; CAUCASIAN; CHILD; DISEASE ACTIVITY; DISEASE COURSE; DISEASE SEVERITY; FAT CONTENT; FEMALE; GENE FREQUENCY; GENE MUTATION; GENETIC SCREENING; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMAN; LIVER BIOPSY; LIVER CELL; LIVER CIRRHOSIS; MAJOR CLINICAL STUDY; MALE; NEUROLOGIC DISEASE; NONALCOHOLIC FATTY LIVER; PATHOGENESIS; PATIENT; PRIORITY JOURNAL; PROTEIN FUNCTION; SINGLE NUCLEOTIDE POLYMORPHISM; WILSON DISEASE; ALLELE; BIOPSY; DNA MUTATIONAL ANALYSIS; GENETIC PREDISPOSITION; GENETICS; LIVER; METABOLISM; MIDDLE AGED; MUTATION; PATHOLOGY; PRESCHOOL CHILD; YOUNG ADULT;

ADOLESCENT; ADULT; ALLELES; BIOPSY; CHILD; CHILD, PRESCHOOL; COPPER; DNA; DNA MUTATIONAL ANALYSIS; FEMALE; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HEPATOLENTICULAR DEGENERATION; HUMANS; LIPASE; LIVER; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MUTATION; YOUNG ADULT;

EID: 84931561642     PISSN: 01688278     EISSN: 16000641     Source Type: Journal    
DOI: 10.1016/j.jhep.2015.01.034     Document Type: Article

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