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

May 30, 2015

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