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Q35933888-59B62F70-D842-4AC0-903B-F0503BF5B5FA
Q35933888-59B62F70-D842-4AC0-903B-F0503BF5B5FA
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http://www.wikidata.org/entity/statement/Q35933888-59B62F70-D842-4AC0-903B-F0503BF5B5FA
Dominant Retinitis Pigmentosa, p.Gly56Arg Mutation in NR2E3: Phenotype in a Large Cohort of 24 Cases
P2860
Q35933888-59B62F70-D842-4AC0-903B-F0503BF5B5FA
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35933888-59B62F70-D842-4AC0-903B-F0503BF5B5FA
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wasDerivedFrom
ef826950a4d53f1c2d37e09798cea1d2dd864649
P2860
Mutation of a nuclear receptor gene, NR2E3, causes enhanced S cone syndrome, a disorder of retinal cell fate.