APA
Audo I., Kohl S., Leroy B. P., Munier F. L., Guillonneau X., Mohand-Saïd S., Bujakowska K., Nandrot E. F., Lorenz B., Preising M., Kellner U., Renner A. B., Bernd A., Antonio A., Moskova-Doumanova V., Lancelot M., Poloschek C. M., Drumare I., Defoort-Dhellemmes S., Wissinger B., Léveillard T., Hamel C. P., Schorderet D. F., De Baere E., Berger W., Jacobson S. G., Zrenner E., Sahel J., Bhattacharya S. S. & Zeitz C. (20091222). TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. : American journal of human genetics.
Chicago
Audo Isabelle, Kohl Susanne, Leroy Bart P, Munier Francis L, Guillonneau Xavier, Mohand-Saïd Saddek, Bujakowska Kinga, Nandrot Emeline F, Lorenz Birgit, Preising Markus, Kellner Ulrich, Renner Agnes B, Bernd Antje, Antonio Aline, Moskova-Doumanova Veselina, Lancelot Marie-Elise, Poloschek Charlotte M, Drumare Isabelle, Defoort-Dhellemmes Sabine, Wissinger Bernd, Léveillard Thierry, Hamel Christian P, Schorderet Daniel F, De Baere Elfride, Berger Wolfgang, Jacobson Samuel G, Zrenner Eberhart, Sahel José-Alain, Bhattacharya Shomi S and Zeitz Christina. 20091222. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. : American journal of human genetics.
Harvard
Audo I., Kohl S., Leroy B. P., Munier F. L., Guillonneau X., Mohand-Saïd S., Bujakowska K., Nandrot E. F., Lorenz B., Preising M., Kellner U., Renner A. B., Bernd A., Antonio A., Moskova-Doumanova V., Lancelot M., Poloschek C. M., Drumare I., Defoort-Dhellemmes S., Wissinger B., Léveillard T., Hamel C. P., Schorderet D. F., De Baere E., Berger W., Jacobson S. G., Zrenner E., Sahel J., Bhattacharya S. S. and Zeitz C. (20091222). TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. : American journal of human genetics.
MLA
Audo Isabelle, Kohl Susanne, Leroy Bart P, Munier Francis L, Guillonneau Xavier, Mohand-Saïd Saddek, Bujakowska Kinga, Nandrot Emeline F, Lorenz Birgit, Preising Markus, Kellner Ulrich, Renner Agnes B, Bernd Antje, Antonio Aline, Moskova-Doumanova Veselina, Lancelot Marie-Elise, Poloschek Charlotte M, Drumare Isabelle, Defoort-Dhellemmes Sabine, Wissinger Bernd, Léveillard Thierry, Hamel Christian P, Schorderet Daniel F, De Baere Elfride, Berger Wolfgang, Jacobson Samuel G, Zrenner Eberhart, Sahel José-Alain, Bhattacharya Shomi S and Zeitz Christina. TRPM1 is mutated in patients with autosomal-recessive complete congenital stationary night blindness. : American journal of human genetics. 20091222.