CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium
Ji Eun Lee(Soonchunhyang University), Joseph G. Gleeson(Children’s Institute), Mitsutoshi Setou(Hamamatsu University School of Medicine), Jesus Olvera(Howard Hughes Medical Institute), Maha S. Zaki(National Water Research Center), Stephanie Bielas(University of Michigan), Miriam Iannicelli(Casa Sollievo della Sofferenza), Clare V. Logan(University of Leeds), Colin A. Johnson(University of Leeds), Hilary R Raynes(Albert Einstein College of Medicine), Francesco Brancati(Piaggio (Italy)), Jana Schroth(Howard Hughes Medical Institute), Andrew M Schlossman(Howard Hughes Medical Institute), Koji Ikegami(Hamamatsu University), Eugen Boltshauser(University of Zurich), Enza Maria Valente(University of Pavia), Barry Merriman(Johns Hopkins University), Sarah Marsh(Howard Hughes Medical Institute), Stanley F. Nelson(University of California, Los Angeles), Andrew Cluckey(University of Michigan), Ian A. Glass(University of Washington), Friedhelm Hildebrandt(Boston Children's Hospital), Clara Barbot(Hospital Maria Pia), Carrie M Louie(University of California San Diego), Jeong Ho Lee(Korea Advanced Institute of Science and Technology), Isabelle Rapin(Johns Hopkins University), Jennifer L. Silhavy(Howard Hughes Medical Institute), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Daniel Doherty(University of Washington), Ignacio P Castroviejo(Hospital Universitario La Paz)
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