TMEM231, mutated in orofaciodigital and Meckel syndromes, organizes the ciliary transition zone
Elle C. Roberson(University of California, San Francisco), Jeremy F. Reiter(Chan Zuckerberg Initiative (United States)), Nadia Elkhartoufi(Hôpital Necker-Enfants Malades), Erica E. Davis(Northwestern University), Sophie Saunier(Hôpital Necker-Enfants Malades), Francesc R. García-Gonzalo(Instituto de Salud Carlos III), Jan Halbritter(Humboldt-Universität zu Berlin), Heidi Cope(Duke University), William E. Dowdle(University of California, San Francisco), Michel R. Leroux(Simon Fraser University), John A. Sayer(Newcastle University), Nicholas Katsanis(Io Therapeutics (United States)), Sophie Thomas(Inserm), Allison E. Ashley‐Koch(Broad Institute), Edgar A. Otto(University of Michigan), Jonathan D. Porath, Ayşegül Ozantürk(Duke University), Friedhelm Hildebrandt(Boston Children's Hospital), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Chunmei Li(Peking University), Simon G. Gregory(Center for Human Genetics)
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