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Q35091262-06C62347-20C9-409A-9747-2E89BC71F7F3
Q35091262-06C62347-20C9-409A-9747-2E89BC71F7F3
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http://www.wikidata.org/entity/statement/Q35091262-06C62347-20C9-409A-9747-2E89BC71F7F3
Mechanistically distinct mouse models for CRX-associated retinopathy.
P2860
Q35091262-06C62347-20C9-409A-9747-2E89BC71F7F3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35091262-06C62347-20C9-409A-9747-2E89BC71F7F3
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wasDerivedFrom
4e846abbd2e4c73a980ee4c1ffcc5b7e30fba4e3
P2860
Autosomal dominant retinal degeneration and bone loss in patients with a 12-bp deletion in the CRX gene