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Q36467228-236B1B23-801D-441B-B4F7-A9FED767BBEE
Q36467228-236B1B23-801D-441B-B4F7-A9FED767BBEE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36467228-236B1B23-801D-441B-B4F7-A9FED767BBEE
Mutations in RPGR and RP2 account for 15% of males with simplex retinal degenerative disease
P2860
Q36467228-236B1B23-801D-441B-B4F7-A9FED767BBEE
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36467228-236B1B23-801D-441B-B4F7-A9FED767BBEE
rank
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wasDerivedFrom
45a1d721f7b41ac3dfaeca40f10eac6744def603
P2860
Gene therapy for leber congenital amaurosis caused by RPE65 mutations: safety and efficacy in 15 children and adults followed up to 3 years.