<i>IFT81</i>, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
Isabelle Perrault(Délégation Paris 5), Friedhelm Hildebrandt(Boston Children's Hospital), Catherine Caillaud(Hôpital Necker-Enfants Malades), Sophie Saunier(Hôpital Necker-Enfants Malades), Meriem Garfa‐Traoré(Délégation Paris 5), Esben Lorentzen(Aarhus University), Jan Halbritter(Humboldt-Universität zu Berlin), Philippe Bastin(Inserm), Daniela A. Braun(University Hospital Münster), Nathalie Boddaert(St Nicholas Hospital), Richard P. Lifton(Rockefeller University), Sophie Thomas(Inserm), Hanan Fathy(Alexandria University), Michael Taschner(Max Planck Institute of Biochemistry), Heon Yung Gee(Yonsei University), Xavier Gérard(Inserm), Edgar A. Otto(University of Michigan), Jean‐Michel Rozet(Inserm), Jonathan D. Porath, Josseline Kaplan(Inserm), Markus Schueler(Boston Children's Hospital), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades), Jennifer A. Lawson(Eugene Research Institute), Valérie Cormier‐Daire(Hôpital Necker-Enfants Malades)
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