The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome
Marion Delous(Université Claude Bernard Lyon 1), Sophie Saunier(Hôpital Necker-Enfants Malades), Kálmán Tory(Délégation Paris 5), Hubert Nivet(Centre Hospitalier Universitaire de Tours), Patrick Niaudet(Hôpital Necker-Enfants Malades), Christelle Golzio(Centre National de la Recherche Scientifique), Flora Silbermann(Délégation Paris 5), Gérard Champion(Centre Hospitalier Universitaire d'Angers), Tiphanie Lacoste(Délégation Paris 5), Catherine Ozilou(Hôpital Necker-Enfants Malades), Christine Laclef(Inserm), Colin A. Johnson(University of Leeds), Férechté Encha‐Razavi(Délégation Paris 5), Lekbir Baala(Délégation Paris 5), Jeanette Vierkotten(Heinrich Heine University Düsseldorf), Rémi Salomon(Inserm), Jean Pierre Berthélémé(ManRos Therapeutics (France)), Nathalie Boddaert(St Nicholas Hospital), Imane Moutkine(Inserm), Eleanor Rattenberry(Birmingham Women's Hospital), Christine Vesque(Centre National de la Recherche Scientifique), Matthias T. F. Wolf(Children's Medical Center), Isabelle Anselme(Centre National de la Recherche Scientifique), Corinne Antignac(Hôpital Necker-Enfants Malades), Marie-Claire Gübler(Inserm), Friedhelm Hildebrandt(Boston Children's Hospital), Jéléna Martinovic(Hôpital Necker-Enfants Malades), Ulrich Rüther(Heinrich Heine University Düsseldorf), Sylvie Schneider‐Maunoury(Centre National de la Recherche Scientifique), Christoph Gerhardt(University of Potsdam), Nathan E. Hellman(University of Pennsylvania), Fiona McDonald(Royal Marsden Hospital), Laurianne Besse(King's College London), Marie Alice Macher(Assistance Publique – Hôpitaux de Paris), Michel Vekemans(Hôpital Necker-Enfants Malades), Marie Gonzalès(Sorbonne Université), Tania Attié‐Bitach(Hôpital Necker-Enfants Malades)
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