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Q36228224-6FB5AC88-35A4-4F0F-AC5D-C1A00457C8A0
Q36228224-6FB5AC88-35A4-4F0F-AC5D-C1A00457C8A0
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http://www.wikidata.org/entity/statement/Q36228224-6FB5AC88-35A4-4F0F-AC5D-C1A00457C8A0
Intragenic Deletions in ATP7B as an Unusual Molecular Genetics Mechanism of Wilson's Disease Pathogenesis.
P2860
Q36228224-6FB5AC88-35A4-4F0F-AC5D-C1A00457C8A0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36228224-6FB5AC88-35A4-4F0F-AC5D-C1A00457C8A0
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wasDerivedFrom
0873eef5e90c751dc4b2e8954278c715918d4e29
P2860
Homozygosity for a gross partial gene deletion of the C-terminal end of ATP7B in a Wilson patient with hepatic and no neurological manifestations.