The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene
Tanzi, R.E. ; Petrukhin, K. ; Chernov, I. ; Pellequer, J.L. ; Wasco, W. ; Ross, B. ; Romano, D.M. ; Parano, E. ; Pavone, L. ; Brzustowicz, L.M. ; Devoto, M. ; Peppercorn, J. ; Bush, A.I. ; Sternlieb, I. ; Pirastu, M. ; Gusella, J.F. ; Evgrafov, O. ; Penchaszadeh, G.K. ; Honig, B. ; Edelman, I.S. ; Soares, M.B. ; Scheinberg, I.H. ; Gilliam, T.C.
[s.l.] : Nature Publishing Group
Published 1993
[s.l.] : Nature Publishing Group
Published 1993
| ISSN: |
1546-1718
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| Source: |
Nature Archives 1869 - 2009
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| Topics: |
Biology
Medicine
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| Notes: |
[Auszug] Wilson disease (WD) is an autosomal recessive disorder characterized by the toxic accumulation of copper in a number of organs, particularly the liver and brain. As shown in the accompanying paper, linkage disequilibrium & haplotype analysis confirmed the disease locus to a single marker ...
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| Type of Medium: |
Electronic Resource
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| URL: |