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Q24300726-05D82210-C222-4C5A-A010-A6867063DD64
Q24300726-05D82210-C222-4C5A-A010-A6867063DD64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24300726-05D82210-C222-4C5A-A010-A6867063DD64
Disruption of the basal body protein POC1B results in autosomal-recessive cone-rod dystrophy
P2860
Q24300726-05D82210-C222-4C5A-A010-A6867063DD64
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24300726-05D82210-C222-4C5A-A010-A6867063DD64
rank
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wasDerivedFrom
96ca1bdae589fff8fab4f7c20e59f1c50abf02db
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis