Mutations in <i>CEP120</i> cause Joubert syndrome as well as complex ciliopathy phenotypes
Susanne Roosing(Radboud University Nijmegen), Enza Maria Valente(University of Pavia), Andrea Poretti(Johns Hopkins University), Ratna Dua Puri(Sir Ganga Ram Hospital), Marta Romani, Hülya Kayserili(Istanbul University), Philippe Moerman(KU Leuven), Lihadh Al‐Gazali(United Arab Emirates University), Umut Altunoğlu(Istanbul University), Alessia Micalizzi(University of Messina), Stefano D’Arrigo(Areté Associates (United States)), Hilde Van Esch, Trudy McKanna(Spectrum Health), Eugen Boltshauser(University of Zurich), Tommaso Mazza(Casa Sollievo della Sofferenza), Paul R. Mark(Spectrum Health), B. De Keersmaecker(AZ Groeninge), Mala Isrie(VIB-KU Leuven Center for Cancer Biology), Joachim Van Keirsbilck(KU Leuven), Sarah Brandenberger(Spectrum Health), Joseph G. Gleeson(Children’s Institute), Damir Musaev(Yale University), Rasim Özgür Rosti(Istanbul University), Ichraf Kraoua(National Institute of Neurology Mongi-Ben Hamida)
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