Mutations in the Cilia Gene ARL13B Lead to the Classical Form of Joubert Syndrome
Vincent Cantagrel(Inserm), Joseph G. Gleeson(Children’s Institute), Sophie Audollent(Hôpital Necker-Enfants Malades), Stephanie Bielas(University of Michigan), Clare V. Logan(University of Leeds), Dominika Swistun(Howard Hughes Medical Institute), Julien Bertrand(University of Geneva), Colin A. Johnson(University of Leeds), Lihadh Al‐Gazali(United Arab Emirates University), Francesco Brancati(Piaggio (Italy)), William B. Dobyns(University of Minnesota), C. Geoffrey Woods(University of Cambridge), David Traver(University of California San Diego), Edgar A. Otto(University of Michigan), Enza Maria Valente(University of Pavia), Sarah Marsh(Howard Hughes Medical Institute), Ian A. Glass(University of Washington), Friedhelm Hildebrandt(Boston Children's Hospital), Bassam R. Ali(Abu Dhabi University), Christopher Bennett(Duke University), Tamara Caspary(Emory University), Jennifer L. Silhavy(Howard Hughes Medical Institute), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Kenton R. Holden, Tom H. Lindner(University Hospital Leipzig)
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