An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
scientific article published on 27 July 2016
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author: Anne Kurtenbach, Crystel Bonnet, Lisbeth Birk Møller, Aziz El-Amraoui, Susanne Kohl, Sandro Banfi, Isabelle Audo, Christine Petit, José-Alain Sahel, Jean-Pierre Hardelin, Gaëlle M Lefevre, Sandrine Marlin, Sandra Chantot-Bastaraud, Alberto Auricchio, Francesca Simonelli, Ieva Sliesoraityte, Saddek Mohand-Saïd, Mélanie Letexier, Amrit Singh-Estivalet
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