TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

著者: Isabelle Audo, Susanne Kohl, Bart P. Leroy, Francis L. Munier, Xavier Guillonneau, Saddek Mohand‐Saïd, Kinga M. Bujakowska, Emeline F. Nandrot, Birgit Lorenz, Markus N. Preising, Ulrich Kellner, Agnes B. Renner, Antje Bernd, Aline Antonio, Veselina Moskova‐Doumanova, Marie‐Elise Lancelot, Charlotte M. Poloschek, Isabelle Drumare, Sabine Defoort‐Dhellemmes, Bernd Wissinger, Thierry Léveillard, Christian Hamel, Daniel F. Schorderet, Elfride De Baere, Wolfgang Berger, Samuel G. Jacobson, Eberhart Zrenner, José‐Alain Sahel, Shomi S. Bhattacharya, Christina Zeitz - The American Journal of Human Genetics 2009 被引用: 262