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Q24308692-F6E1A94D-9771-4B16-BBB3-3719B739BE59
Q24308692-F6E1A94D-9771-4B16-BBB3-3719B739BE59
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Statement
http://www.wikidata.org/entity/statement/Q24308692-F6E1A94D-9771-4B16-BBB3-3719B739BE59
Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome
P2860
Q24308692-F6E1A94D-9771-4B16-BBB3-3719B739BE59
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24308692-F6E1A94D-9771-4B16-BBB3-3719B739BE59
rank
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wasDerivedFrom
8eece7152868e4ccc389cde222bb57591f91f0de
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis