Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome

  • Susanne Roosing
  • , Matan Hofree
  • , Sehyun Kim
  • , Eric Scott
  • , Brett Copeland
  • , Marta Romani
  • , Jennifer L. Silhavy
  • , Rasim O. Rosti
  • , Jana Schroth
  • , Tommaso Mazza
  • , Elide Miccinilli
  • , Maha S. Zaki
  • , Kathryn J. Swoboda
  • , Joanne Milisa-Drautz
  • , William B. Dobyns
  • , Mohamed Mikati
  • , Faruk İncecik
  • , Matloob Azam
  • , Renato Borgatti
  • , Romina Romaniello
    • Rose Mary Boustany, Carol L. Clericuzio, Stefano D’Arrigo, Petter Strømme, Eugen Boltshauser, Franco Stanzial, Marisol Mirabelli-Badenier, Isabella Moroni, Enrico Bertini, Francesco Emma, Maja Steinlin, Friedhelm Hildebrandt, Colin A. Johnson, Michael Freilinger, Keith K. Vaux, Stacey B. Gabriel, Pedro Aza-Blac, Susanne Genel Heynen, Trey Ideker, Brian D. Dynlacht, Ji Eun Lee, Enza Maria Valente, Joon Kim, Joseph G. Gleeson

Research output: Contribution to journal › Article › peer-review

67 Scopus citations

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Keyphrases

Biochemistry, Genetics and Molecular Biology