The Copper-Transporting ATpase Defective in Wilson Disease
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Publisher
Springer US
Link
http://link.springer.com/content/pdf/10.1007/978-1-4615-4723-5_19.pdf
Reference50 articles.
1. Bull, P.C., Barwell, J.A., Hannah, H.T-L., Pautler, S.E., Higgins, M.J., Lalande, M., and Cox, D.W. (1993). Isolation of new probes in the region of the Wilson disease locus, 13q 14.2-14.3. Cytogenet. Cell Genet. 64,12–17.
2. Bull, P.C. and Cox, D.W. (1994). Wilson disease and Menkes disease: new handles on heavy-metal transport. Trends Genet. 10,246–252.
3. Bull, P.C., Thomas, G.R., Rommens, J.M., Forbes, J.R., and Cox, D.W. (1993). The Wilson disease gene is a putative copper transporting P-type ATPase similar to the Menkes gene erratum appears in Nat Genet 1994 6:214. Nature Genet. 5, 327–337.
4. Cauza, E., Maier-Dobersberger, T., Polli, C, Kaserer, K., Kramer, L., and Ferenci, P. (1997). Screening for wilson’ disease in patients with liver diseases by serum ceruloplasmin. J. Hepatol. 27,358–362.
5. Chelly, J., Turner, Z., Tonnesen, T., Petterson, A., Ishikawa-Brush, Y., Tommerup, N., Horn, N., and Monaco, A.P. (1993). Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding protein. Nature Genet. 3,14–19.
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