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Q35769930-B325334C-4CD0-45F8-A580-C8EED3474B19
Q35769930-B325334C-4CD0-45F8-A580-C8EED3474B19
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http://www.wikidata.org/entity/statement/Q35769930-B325334C-4CD0-45F8-A580-C8EED3474B19
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
P2860
Q35769930-B325334C-4CD0-45F8-A580-C8EED3474B19
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35769930-B325334C-4CD0-45F8-A580-C8EED3474B19
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wasDerivedFrom
6d2e941129102899615b1c0879a26dad45db6d85
P2860
Mutations in B9D1 and MKS1 cause mild Joubert syndrome: expanding the genetic overlap with the lethal ciliopathy Meckel syndrome.