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Q33938150-80309B77-0833-4B29-8630-9BD47DAAE095
Q33938150-80309B77-0833-4B29-8630-9BD47DAAE095
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33938150-80309B77-0833-4B29-8630-9BD47DAAE095
Mutation discovered in a feline model of human congenital retinal blinding disease.
P2860
Q33938150-80309B77-0833-4B29-8630-9BD47DAAE095
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33938150-80309B77-0833-4B29-8630-9BD47DAAE095
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wasDerivedFrom
5600458b636e45a19f01d5ea0d60fbdad341f4d7
P2860
De novo mutations in the CRX homeobox gene associated with Leber congenital amaurosis