Search All UT System Experts

The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome

Marion Delous, Lekbir Baala, Rémi Salomon, Christine Laclef, Jeanette Vierkotten, Kàlmàn Tory, Christelle Golzio, Tiphanie Lacoste, Laurianne Besse, Catherine Ozilou, Imane Moutkine, Nathan E. Hellman, Isabelle Anselme, Flora Silbermann, Christine Vesque, Christoph Gerhardt, Eleanor Rattenberry, Matthias T F Wolf, Marie Claire Gubler, Jéléna MartinovicFéréchté Encha-Razavi, Nathalie Boddaert, Marie Gonzales, Marie Alice Macher, Hubert Nivet, Gérard Champion, Jean Pierre Berthélémé, Patrick Niaudet, Fiona McDonald, Friedhelm Hildebrandt, Colin A. Johnson, Michel Vekemans, Corinne Antignac, Ulrich Rüther, Sylvie Schneider-Maunoury, Tania Attié-Bitach, Sophie Saunier

Research output: Contribution to journal › Article › peer-review

389 Scopus citations

Fingerprint

Dive into the research topics of 'The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome'. Together they form a unique fingerprint.

Medicine & Life Sciences