Showing results 3 to 4 of 4
Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome Roosing, Susanne; Hofree, Matan; Kim, Sehyun; Scott, Eric; Copeland, Brett; Romani, Marta; Silhavy, Jennifer L; et al, ELIFE, v.4, 2015-05 |
Mutations in TMEM216 perturb ciliogenesis and cause Joubert, Meckel and related syndromes Valente, Enza Maria; Logan, Clare V.; Mougou-Zerelli, Soumaya; Lee, Jeong Ho; Silhavy, Jennifer L.; Brancati, Francesco; Iannicelli, Miriam; et al, NATURE GENETICS, v.42, no.7, pp.619 - 625, 2010-07 |
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