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Q33938150-CE9F53C0-4670-4CF2-A083-34079F838C2E
Q33938150-CE9F53C0-4670-4CF2-A083-34079F838C2E
BestRank
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http://www.wikidata.org/entity/statement/Q33938150-CE9F53C0-4670-4CF2-A083-34079F838C2E
Mutation discovered in a feline model of human congenital retinal blinding disease.
P2860
Q33938150-CE9F53C0-4670-4CF2-A083-34079F838C2E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33938150-CE9F53C0-4670-4CF2-A083-34079F838C2E
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wasDerivedFrom
5600458b636e45a19f01d5ea0d60fbdad341f4d7
P2860
A range of clinical phenotypes associated with mutations in CRX, a photoreceptor transcription-factor gene.