Advanced search
Add to list

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

Author
Organization

Citation

Please use this url to cite or link to this publication:

MLA
Audo, I et al. “TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness.” AMERICAN JOURNAL OF HUMAN GENETICS 85.5 (2009): 720–729. Print.
APA
Audo, I., Kohl, S., Leroy, B., Munier, F., Guillonneau, X., Mohand-Saïd, S., Bujakowska, K., et al. (2009). TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. AMERICAN JOURNAL OF HUMAN GENETICS, 85(5), 720–729.
Chicago author-date
Audo, I, S Kohl, Bart Leroy, FL Munier, X Guillonneau, S Mohand-Saïd, K Bujakowska, et al. 2009. “TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness.” American Journal of Human Genetics 85 (5): 720–729.
Chicago author-date (all authors)
Audo, I, S Kohl, Bart Leroy, FL Munier, X Guillonneau, S Mohand-Saïd, K Bujakowska, E Nandrot, B Lorenz, M Preising, U Kellner, A Renner, A Bernd, A Antonio, M Moskova-Doumanova, ME Lancelot, CM Poloschek, I Drumare, S Defoort-Dhellemmes, B Wissinger, T Léveillard, CP Hamel, DF Schroderet, Elfride De Baere, W Berger, SG Jacobson, E Zrenner, JA Sahel, SS Battacharya, and C Zeitz. 2009. “TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness.” American Journal of Human Genetics 85 (5): 720–729.
Vancouver
1.
Audo I, Kohl S, Leroy B, Munier F, Guillonneau X, Mohand-Saïd S, et al. TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness. AMERICAN JOURNAL OF HUMAN GENETICS. Cambridge: Cell Press; 2009;85(5):720–9.
IEEE
[1]
I. Audo et al., “TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness,” AMERICAN JOURNAL OF HUMAN GENETICS, vol. 85, no. 5, pp. 720–729, 2009.
@article{953331,
  author       = {Audo, I and Kohl, S and Leroy, Bart and Munier, FL and Guillonneau, X and Mohand-Saïd, S and Bujakowska, K and Nandrot, E and Lorenz, B and Preising, M and Kellner, U and Renner, A and Bernd, A and Antonio, A and Moskova-Doumanova, M and Lancelot, ME and Poloschek, CM and Drumare, I and Defoort-Dhellemmes, S and Wissinger, B and Léveillard, T and Hamel, CP and Schroderet, DF and De Baere, Elfride and Berger, W and Jacobson, SG and Zrenner, E and Sahel, JA and Battacharya, SS and Zeitz, C},
  issn         = {0002-9297},
  journal      = {AMERICAN JOURNAL OF HUMAN GENETICS},
  language     = {eng},
  number       = {5},
  pages        = {720--729},
  publisher    = {Cell Press},
  title        = {TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness},
  url          = {http://dx.doi.org/10.1016/j.ajhg.2009.10.013},
  volume       = {85},
  year         = {2009},
}

Altmetric
View in Altmetric
Web of Science
Times cited: