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Q24307529-006F2C5D-B418-492F-80B8-E1CB542FE0ED
Q24307529-006F2C5D-B418-492F-80B8-E1CB542FE0ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-006F2C5D-B418-492F-80B8-E1CB542FE0ED
RP1L1 variants are associated with a spectrum of inherited retinal diseases including retinitis pigmentosa and occult macular dystrophy
P2860
Q24307529-006F2C5D-B418-492F-80B8-E1CB542FE0ED
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24307529-006F2C5D-B418-492F-80B8-E1CB542FE0ED
rank
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Statement
wasDerivedFrom
eb30a7564f8ab792f8f1ff5c63c5f4d34753da39
P2860
Essential and synergistic roles of RP1 and RP1L1 in rod photoreceptor axoneme and retinitis pigmentosa