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Q35091262-1E6CA2E0-33C3-4EBC-9FDB-0A1FC4CB7562
Q35091262-1E6CA2E0-33C3-4EBC-9FDB-0A1FC4CB7562
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Statement
http://www.wikidata.org/entity/statement/Q35091262-1E6CA2E0-33C3-4EBC-9FDB-0A1FC4CB7562
Mechanistically distinct mouse models for CRX-associated retinopathy.
P2860
Q35091262-1E6CA2E0-33C3-4EBC-9FDB-0A1FC4CB7562
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35091262-1E6CA2E0-33C3-4EBC-9FDB-0A1FC4CB7562
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wasDerivedFrom
4e846abbd2e4c73a980ee4c1ffcc5b7e30fba4e3
P2860
Evidence of autosomal dominant Leber congenital amaurosis (LCA) underlain by a CRX heterozygous null allele.