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Q27319191-71513F43-F2C0-4871-AA8C-69C7174E584A
Q27319191-71513F43-F2C0-4871-AA8C-69C7174E584A
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http://www.wikidata.org/entity/statement/Q27319191-71513F43-F2C0-4871-AA8C-69C7174E584A
Investigating embryonic expression patterns and evolution of AHI1 and CEP290 genes, implicated in Joubert syndrome
P2860
Q27319191-71513F43-F2C0-4871-AA8C-69C7174E584A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q27319191-71513F43-F2C0-4871-AA8C-69C7174E584A
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wasDerivedFrom
9510015c8a5a9067a765c9e7edbb2d7271427c53
P2860
Mutations in the CEP290 (NPHP6) gene are a frequent cause of Leber congenital amaurosis