Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation
1998 ◽
Vol 95
(18)
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pp. 10854-10859
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2008 ◽
Vol 383
(5)
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pp. 1097-1111
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Keyword(s):
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1997 ◽
Vol 272
(34)
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pp. 21461-21466
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2007 ◽
Vol 282
(12)
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pp. 8622-8631
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2008 ◽
Vol 173
(6)
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pp. 1783-1794
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