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Three novel mutations (P760L, L1305P, Q1351Stop) causing Wilson disease.

Human mutation - 1 Feb 2001

Genschel J, Czlonkowska A, Sommer G, Buettner C, Bochow B, Lochs H, Schmidt H

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PMID: 11180609
DOI: 10.1002/1098-1004(200102)17:2<156::AID-HUMU18>3.0.CO;2-0

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