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Q24678616-94283B75-1970-4259-B7E8-7145625FDEDC
Q24678616-94283B75-1970-4259-B7E8-7145625FDEDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24678616-94283B75-1970-4259-B7E8-7145625FDEDC
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis
P2860
Q24678616-94283B75-1970-4259-B7E8-7145625FDEDC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24678616-94283B75-1970-4259-B7E8-7145625FDEDC
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wasDerivedFrom
43f5542797691a5b599b64a4fa2226b26b9d0f96
P2860
Mutations in CEP290, which encodes a centrosomal protein, cause pleiotropic forms of Joubert syndrome