CC2D2A Is Mutated in Joubert Syndrome and Interacts with the Ciliopathy-Associated Basal Body Protein CEP290
Nicholas T. Gorden(University of Washington), Dan Doherty(University of Washington), Erica E. Davis(Northwestern University), Elaine H. Zackai(Children's Hospital of Philadelphia), Dana Knutzen(University of Washington), Edwin W. Rubel(University of Virginia Medical Center), David W. Raible(University of Washington Medical Center), Theo K. Bammler(University of Washington), John B. Vincent(Centre for Addiction and Mental Health), Heleen H. Arts(Radboud University Nijmegen), Nicholas Katsanis(Io Therapeutics (United States)), Carolyn M. Hutter(National Human Genome Research Institute), Abigail Hikida(University of Washington), Hamìt Özyürek(Ondokuz Mayıs University), Abdulrahman Alswaid(King Abdulaziz Medical City), Sylvia E. C. van Beersum(Radboud University Nijmegen), Ronald Roepman(Radboud University Nijmegen), Edgar A. Otto(University of Michigan), Melissa Eckert(University of California, Davis), Karlien L. M. Coene(Radboud University Nijmegen), Sel Dibooğlu(University of Missouri–St. Louis), Nine V.A.M. Knoers(University Medical Center Groningen), Ian A. Glass(University of Washington), Friedhelm Hildebrandt(Boston Children's Hospital), Dorus A. Mans(Radboud University Nijmegen), Meral Topçu(Hacettepe University Hospital), Cecilia B. Moens(Fred Hutch Cancer Center), Yangfan Liu, Michael O. Dorschner(University of Washington), Stef J.F. Letteboer(Radboud University Nijmegen), Phillip F. Chance(University of Utah), Frederico M. Farin(University of Washington), Melissa A. Parisi(University of Washington), Kelly N. Owens(University of Washington), Phillip Rosenthal(San Francisco General Hospital)
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