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2017 | 1 |
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Null mutation of the murine ATP7B (Wilson disease) gene results in intracellular copper accumulation and late-onset hepatic nodular transformation.
Hum Mol Genet. 1999 Sep;8(9):1665-71. doi: 10.1093/hmg/8.9.1665.
Hum Mol Genet. 1999.
PMID: 10441329
Targeted inactivation of copper transporter Atp7b in hepatocytes causes liver steatosis and obesity in mice.
Muchenditsi A, Yang H, Hamilton JP, Koganti L, Housseau F, Aronov L, Fan H, Pierson H, Bhattacharjee A, Murphy R, Sears C, Potter J, Wooton-Kee CR, Lutsenko S.
Muchenditsi A, et al.
Am J Physiol Gastrointest Liver Physiol. 2017 Jul 1;313(1):G39-G49. doi: 10.1152/ajpgi.00312.2016. Epub 2017 Apr 20.
Am J Physiol Gastrointest Liver Physiol. 2017.
PMID: 28428350
Free PMC article.
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