Cite
A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness
MLA
Riazuddin, S.Amer, et al. “A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness.” American Journal of Human Genetics, vol. 87, no. 4, Oct. 2010, pp. 523–31. EBSCOhost, https://doi.org/10.1016/j.ajhg.2010.08.013.
APA
Riazuddin, S. A., Shahzadi, A., Zeitz, C., Ahmed, Z. M., Ayyagari, R., Chavali, V. R. M., Ponferrada, V. G., Audo, I., Michiels, C., Lancelot, M.-E., Nasir, I. A., Zafar, A. U., Khan, S. N., Husnain, T., Jiao, X., MacDonald, I. M., Riazuddin, S., Sieving, P. A., Katsanis, N., & Hejtmancik, J. F. (2010). A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness. American Journal of Human Genetics, 87(4), 523–531. https://doi.org/10.1016/j.ajhg.2010.08.013
Chicago
Riazuddin, S. Amer, Amber Shahzadi, Christina Zeitz, Zubair M. Ahmed, Radha Ayyagari, Venkata R.M. Chavali, Virgilio G. Ponferrada, et al. 2010. “A Mutation in SLC24A1 Implicated in Autosomal-Recessive Congenital Stationary Night Blindness.” American Journal of Human Genetics 87 (4): 523–31. doi:10.1016/j.ajhg.2010.08.013.