Filter Filter By date Start date End date By Team Michel Polak Alessandra Pierani Patrick Revy & Erika Brunet Sigolène Meilhac Laurent Abel Jeanne Amiel et Laurence Legeai‑Mallet Antonio Rausell Isabelle André Vincent Cantagrel Jean-Laurent Casanova Nadine Cerf-Bensussan Yanick Crow Olivier Hermine & Thiago Trovati Maciel Alain Hovnanian Edor Kabashi Sylvain Latour Valérie Cormier-Daire Mickaël Ménager Gaël Ménasché et Fernando Sepulveda Annarita Miccio Frédéric Rieux-Laucat Agnès Rötig Jean-Michel Rozet Sophie Saunier et Corinne Antignac Matias Simons Nathalie Boddaert Sabine Sarnacki et Isabelle Bloch Yves Ville Yakov VITRENKO Patrick Nitschké Corinne Cordier Meriem Garfa-Traoré Sylvie Fabrega Marie-Alexandra Alyanakian Sophie Berissi Chiara Guerrera Pierre David Nathalie Lefort Claude Besmond Marcelo Simon Sola LEAT Nathalie Boddaert Travail en collaboration : Unité de Recherche clinique-Centre d’investigation clinique (URC-CIC) Travail en collaboration : Département de Biothérapie, Centre d'Investigation Clinique pour les Thérapies Innovantes Salma Kotti Nicolas Garcelon Mickaël Ménager Michela Deleidi Annarita Miccio Annarita Miccio Jean Michel Rozet Sara Bizzotto Elodie Bal Bana Jabri Hossein Khonsari Karim Wahbi Lucile Couronné Denis Jabaudon, Thomas Blauwblomme et Rima Nabbout Bana Jabri Céline GRECO Filter Reset 0 results match your search. Publications Nonsyndromic Retinal Dystrophy due to Bi-Allelic Mutations in the Ciliary... Publications IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy... Publications Intravitreal Injection of Splice-switching Oligonucleotides to Manipulate... Publications Mutations in DOCK7 in individuals with epileptic encephalopathy and cortical... Publications Mutations in NMNAT1 cause Leber congenital amaurosis with early-onset severe... Publications AON-mediated Exon Skipping Restores Ciliation in Fibroblasts Harboring... Publications Mainzer-Saldino syndrome is a ciliopathy caused by IFT140 mutations. Publications TMEM126A, encoding a mitochondrial protein, is mutated in autosomal-recessive... Publications Retinal dehydrogenase 12 (RDH12) mutations in leber congenital amauros... Publications Leber congenital amaurosis--genotyping required for possible inclusion... Newsletter Discoveries, advances, portaits... Find out the latest research news and medical innovations. Votre email Valider Data Privacy Policy
