Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation

Human Molecular Genetics

Volumn 8, Issue 9, 1999, Pages 1665-1671

  Buiakova, Olesia I ^b   Xu, Jin ^b   Lutsenko, Svetlana ^d   Zeitlin, Scott ^a   Das, Kamna ^a   Das, Shonit ^c   Ross, Barbara M ^a   Mekios, Constantinos ^a   Scheinberg, I Herbert ^c   Gilliam, T Conrad ^a,b  

^a Dept of Genetics and Development ^*  (United States)

^b New York Presbyterian Columbia University Medical Center   (United States)

^c ST LUKE S ROOSEVELT HOSPITAL CENTER   (United States)

^d OREGON HEALTH AND SCIENCE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATASE; COPPER;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; BRAIN; CONTROLLED STUDY; GENE MUTATION; KIDNEY; LIVER CIRRHOSIS; LIVER NODULE; MAMMARY GLAND; MILK; MOUSE; NONHUMAN; PHENOTYPE; PLACENTA; PRIORITY JOURNAL; PROGENY; WILSON DISEASE;

ADENOSINE TRIPHOSPHATASES; ANIMALS; ANIMALS, NEWBORN; CARRIER PROTEINS; CATION TRANSPORT PROTEINS; COPPER; FIBROSIS; HEPATOLENTICULAR DEGENERATION; HOMOZYGOTE; LIVER; MICE; MICE, KNOCKOUT; MUTATION; PHENOTYPE;

ANIMALIA; MURINAE; RODENTIA;

EID: 0032878550     PISSN: 09646906     EISSN: None     Source Type: Journal    
DOI: 10.1093/hmg/8.9.1665     Document Type: Article

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