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Q45886746-26DB30FB-5AF7-4F58-B5F2-7F7C18061BA3
Q45886746-26DB30FB-5AF7-4F58-B5F2-7F7C18061BA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45886746-26DB30FB-5AF7-4F58-B5F2-7F7C18061BA3
Retinal optogenetic therapies: clinical criteria for candidacy.
P2860
Q45886746-26DB30FB-5AF7-4F58-B5F2-7F7C18061BA3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q45886746-26DB30FB-5AF7-4F58-B5F2-7F7C18061BA3
rank
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Statement
wasDerivedFrom
61fbf1619da0344560af52a9e9d60c9d15f9867b
P2860
CERKL mutations cause an autosomal recessive cone-rod dystrophy with inner retinopathy.