Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
- Howard Hughes Medical Institute, The Rockefeller University, United States
- University of California, San Diego, United States
- Mendel Institute, Italy
- National Research Center, Egypt
- University of Utah School of Medicine, United States
- University of New Mexico, United States
- Seattle Children's Hospital, United States
- Duke Institute for Brain Sciences, Duke University Medical Center, United States
- Cukurova University Medical Faculty, Turkey
- Wah Medical College, Pakistan
- Scientific Institute IRCCS Eugenio Medea, Italy
- American University of Beirut Medical Center, Lebanon
- Fondazione IRCCS Istituto Neurologico Carlo Besta, Italy
- Oslo University Hospital, Norway
- University Children's Hospital, Switzerland
- Regional Hospital of Bolzano, Italy
- Istituto G. Gaslini, Italy
- Bambino Gesù Children's Research Hospital, IRCCS, Italy
- Bambino Gesù Children's Hospital, IRCCS, Italy
- University Children's Hospital,, Switzerland
- Howard Hughes Medical Institute, Harvard Medical School, United States
- University of Leeds, St. James's University Hospital, United Kingdom
- Medical University Vienna, Austria
- Broad Institute of Harvard and Massachusetts Institute of Technology, United States
- Burnham Institute, United States
- New York University School of Medicine, United States
- Department of Pathology and Cancer Institute, Smilow Research Center, United States
- Sungkyunkwan University, Republic of Korea
- School of Medical Science and Engineering, Republic of Korea
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Functional genome-wide siRNA screen identifies KIAA0586 as mutated in Joubert syndrome
eLife 4:e06602.
https://doi.org/10.7554/eLife.06602
