TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness.
30 auth. I. Audo, S. Kohl, B. Leroy, F. Munier, X. Guillonneau, S. Mohand-Saïd, K. Bujakowska, E. Nandrot, B. Lorenz, M. Preising, U. Kellner, A. Renner, A. Bernd, A. Antonio, V. Moskova-Doumanova, ... Marie‐Elise Lancelot, C. Poloschek, I. Drumare, S. Defoort‐Dhellemmes, B. Wissinger, T. Léveillard, C. Hamel, D. Schorderet, E. de Baere, W. Berger, S. Jacobson, E. Zrenner, J. Sahel, S. Bhattacharya, C. Zeitz