An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
Crystel Bonnet(Centre National de la Recherche Scientifique), Christine Petit(Inserm), Anne Kurtenbach(STZ eyetrial), Saba Battelino(University of Ljubljana), Francesca Simonelli(University of Naples Federico II), Loreto Martorell(Hospital Sant Joan de Déu Barcelona), Susanne Kohl(STZ eyetrial), Isabelle Audo(Inserm), Jaume Catalá‐Mora(Hospital Sant Joan de Déu Barcelona), G. Lefèvre(Centre National de la Recherche Scientifique), Jean‐Pierre Hardelin(Inserm), Mélanie Letexier(Genopole (France)), Luce Smagghe(Institut de la Vision), Sandro Banfi(Telethon Institute Of Genetics And Medicine), Sandrine Marlin(Hôpital Necker-Enfants Malades), A. Amraoui(Centre National de la Recherche Scientifique), Martina Jarc-Vidmar(Ljubljana University Medical Centre), M.A. Clavería(Hospital Sant Joan de Déu Barcelona), Damjan Glavač(University of Ljubljana), Jesus Rodriguez Jorge(Hospital Sant Joan de Déu Barcelona), Francesco Testa(University of Naples Federico II), Ana Fakin(University of Ljubljana), Shzeena Dad(Kennedy Center), Andrej Zupan(University of Ljubljana), Charles Marcaillou(Genopole (France)), Ieva Sliesoraitytė(Centre hospitalier national d'ophtalmologie des Quinze-Vingts), José‐Alain Sahel(University of Pittsburgh), Souad Gherbi, Ditta Zobor(STZ eyetrial), Sandra Chantot‐Bastaraud(Fondation de Rothschild), Zied Riahi(Institut de la Vision), Saddek Mohand‐Saïd(Institut de la Vision), Eberhart Zrenner(STZ eyetrial), Marko Hawlina(Ljubljana University Medical Centre), Lisbeth Birk Møller(Aalborg University Hospital), Amrit Singh‐Estivalet(Centre National de la Recherche Scientifique), Alberto Auricchio(Federico II University Hospital)
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