Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness

MLA

Ajoy Vincent, et al. “Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.” The American Journal of Human Genetics, no. 5, pp. 1011–19. EBSCOhost, https://doi.org/10.1016/j.ajhg.2016.03.021. Accessed 12 Nov. 2024.

APA

Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T. Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, Christelle Michiels, Christel Condroyer, Heather MacDonald, Robert Verdet, José-Alain Sahel, Christian P. Hamel, Christina Zeitz, Elise Héon, Eyal Banin, Beatrice Bocquet, Elfride De Baere, Ingele Casteels, … Xavier Zanlonghi. (n.d.). Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness. The American Journal of Human Genetics, 5, 1011–1019. https://doi.org/10.1016/j.ajhg.2016.03.021

Chicago

Ajoy Vincent, Isabelle Audo, Erika Tavares, Jason T. Maynes, Anupreet Tumber, Thomas Wright, Shuning Li, et al. 2024. “Biallelic Mutations in GNB3 Cause a Unique Form of Autosomal-Recessive Congenital Stationary Night Blindness.” The American Journal of Human Genetics, no. 5: 1011–19. Accessed November 12. doi:10.1016/j.ajhg.2016.03.021.