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Q24676633-A74AF6FC-4C4F-42D1-BBB3-AD4500B7961B
Q24676633-A74AF6FC-4C4F-42D1-BBB3-AD4500B7961B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676633-A74AF6FC-4C4F-42D1-BBB3-AD4500B7961B
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders
P2860
Q24676633-A74AF6FC-4C4F-42D1-BBB3-AD4500B7961B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24676633-A74AF6FC-4C4F-42D1-BBB3-AD4500B7961B
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Statement
wasDerivedFrom
f76e308dc8f57d8005cb58a52f62413469dc7a96
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis