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Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
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Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome.
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome. Elife. 2015 May 30; 4:e06602.
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PubMed
subject areas
Abnormalities, Multiple
Cell Cycle Proteins
Cerebellum
Eye Abnormalities
Gene Frequency
Genetic Predisposition to Disease
Genetic Testing
Genome-Wide Association Study
Heterozygote
Humans
Kidney Diseases, Cystic
Mutant Proteins
Retina
RNA, Small Interfering
authors with profiles
William B. Dobyns