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Q36848752-06E1CA03-36D2-401E-AC9E-5AEC6CD9DC5D
Q36848752-06E1CA03-36D2-401E-AC9E-5AEC6CD9DC5D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36848752-06E1CA03-36D2-401E-AC9E-5AEC6CD9DC5D
Multimodal imaging in hereditary retinal diseases.
P2860
Q36848752-06E1CA03-36D2-401E-AC9E-5AEC6CD9DC5D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36848752-06E1CA03-36D2-401E-AC9E-5AEC6CD9DC5D
rank
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type
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wasDerivedFrom
04d35b7e9242825ceba3b174f96064d43927b9f6
P2860
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.