Items where Author is "Drumare, Isabelle"

Article

Audo, Isabelle and Bujakowska, Kinga and Orhan, Elise and Poloschek, Charlotte M. and Defoort-Dhellemmes, Sabine and Drumare, Isabelle and Kohl, Susanne and Luu, Tien D. and Lecompte, Odile and Zrenner, Eberhart and Lancelot, Marie-Elise and Antonio, Aline and Germain, Aurore and Michiels, Christelle and Audier, Claire and Letexier, Melanie and Saraiva, Jean-Paul and Leroy, Bart P. and Munier, Francis L. and Mohand-Said, Saddek and Lorenz, Birgit and Friedburg, Christoph and Preising, Markus and Kellner, Ulrich and Renner, Agnes B. and Moskova-Doumanova, Veselina and Berger, Wolfgang and Wissinger, Bernd and Hamel, Christian R. and Schorderet, Daniel F. and De Baere, Elfride and Sharon, Dror and Banin, Eyal and Jacobson, Samuel G. and Bonneau, Dominique and Zanlonghi, Xavier and Le Meur, Guylene and Casteels, Ingele and Koenekoop, Robert and Long, Vernon W. and Meire, Francoise and Prescott, Katrina and de Ravel, Thomy and Simmons, Ian and Nguyen, Hoan and Dollfus, Helene and Poch, Olivier and Leveillard, Thierry and Nguyen-Ba-Charvet, Kim and Sahel, Jose-Alain and Bhattacharya, Shomi S. and Zeitz, Christina (2012) Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness. AMERICAN JOURNAL OF HUMAN GENETICS, 90 (2). pp. 321-330. ISSN 0002-9297

Audo, Isabelle and Kohl, Susanne and Leroy, Bart P. and Munier, Francis L. and Guillonneau, Xavier and Mohand-Said, Saddek and Bujakowska, Kinga and Nandrot, Emeline F. and Lorenz, Birgit and Preising, Markus and Kellner, Ulrich and Renner, Agnes B. and Bernd, Antje and Antonio, Aline and Moskova-Doumanova, Veselina and Lancelot, Marie-Elise and Poloschek, Charlotte M. and Drumare, Isabelle and Defoort-Dhellemmes, Sabine and Wissinger, Bernd and Leveillard, Thierry and Hamel, Christian P. and Schorderet, Daniel F. and De Baere, Elfride and Berger, Wolfgang and Jacobson, Samuel G. and Zrenner, Eberhart and Sahel, Jose-Alain and Bhattacharya, Shomi S. and Zeitz, Christina (2009) TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. AMERICAN JOURNAL OF HUMAN GENETICS, 85 (5). pp. 720-729. ISSN 0002-9297, 1537-6605