Targeted Next Generation Sequencing Identifies Novel Mutations in RP1 as a Relatively Common Cause of Autosomal Recessive Rod-Cone Dystrophy. - El Shamieh, Said; Boulanger-Scemama, Elise; Lancelot, Marie-Elise; Antonio, Aline; Démontant, Vanessa; Condroyer, Christel; Letexier, Mélanie; Saraiva, Jean-Paul; Mohand-Saïd, Saddek; Sahel, José-Alain; Audo, Isabelle; Zeitz, Christina (BioMed Research International, 2015)