Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. (Q40071443)

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Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B.
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    Distinct Wilson's disease mutations in ATP7B are associated with enhanced binding to COMMD1 and reduced stability of ATP7B. (English)
    1 reference
    Prim de Bie
    1 reference
    Bart van de Sluis
    1 reference
    Peter V E van de Berghe
    1 reference
    Patricia Muller
    1 reference
    Ruud Berger
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    Jonathan D Gitlin
    1 reference
    Leo W J Klomp
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    25 July 2007
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    133
    1 reference
    1316-1326
    1 reference
    4
    1 reference

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