Cranioectodermal Dysplasia, Sensenbrenner Syndrome, Is a Ciliopathy Caused by Mutations in the IFT122 Gene
Joanna Walczak‐Sztulpa(Poznan University of Medical Sciences), Andreas W. Kuß(Max Planck Institute for Molecular Genetics), Desmond Brown(Princeton University), Daniel P. S. Osborn(University College London), Danuta Zwołińska(Wroclaw Medical University), Anna Latos‐Bieleńska(Poznan University of Medical Sciences), Jonathan Eggenschwiler(University of Georgia), Raoul C. M. Hennekam(University of Amsterdam), Francesco Emma(Bambino Gesù Children's Hospital), Philip L. Beales(Great Ormond Street Hospital), Andreas Tzschach(Max Planck Institute for Molecular Genetics), Claus Klingenberg(University Hospital of North Norway), Jacek Zachwieja(Poznan University of Medical Sciences), Małgorzata Szczepańska(Poznan University of Medical Sciences), Marian Krawczyński(Poznan University of Medical Sciences), Hans‐Hilger Ropers(Max Planck Institute for Molecular Genetics), Giuliano Torre(Bambino Gesù Children's Hospital), Masoud Garshasbi(Max Planck Institute for Molecular Genetics)
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