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Q34963655-3A3234E7-7526-4486-95D9-5AB87F0A677D
Q34963655-3A3234E7-7526-4486-95D9-5AB87F0A677D
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http://www.wikidata.org/entity/statement/Q34963655-3A3234E7-7526-4486-95D9-5AB87F0A677D
Difference in stability of the N-domain underlies distinct intracellular properties of the E1064A and H1069Q mutants of copper-transporting ATPase ATP7B.
P2860
Q34963655-3A3234E7-7526-4486-95D9-5AB87F0A677D
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http://www.wikidata.org/entity/statement/Q34963655-3A3234E7-7526-4486-95D9-5AB87F0A677D
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7155572e9dd0d4c1c641d899f7120cb6df07b709
P2860
Functional expression of the Wilson disease protein reveals mislocalization and impaired copper-dependent trafficking of the common H1069Q mutation.