Cite
Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.
MLA
Irum, Bushra, et al. “Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.” PLoS ONE, vol. 11, no. 12, Dec. 2016, pp. 1–14. EBSCOhost, https://doi.org/10.1371/journal.pone.0167562.
APA
Irum, B., Khan, S. Y., Ali, M., Daud, M., Kabir, F., Rauf, B., Fatima, F., Iqbal, H., Khan, A. O., Al Obaisi, S., Naeem, M. A., Nasir, I. A., Khan, S. N., Husnain, T., Riazuddin, S., Akram, J., Eghrari, A. O., & Riazuddin, S. A. (2016). Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts. PLoS ONE, 11(12), 1–14. https://doi.org/10.1371/journal.pone.0167562
Chicago
Irum, Bushra, Shahid Y. Khan, Muhammad Ali, Muhammad Daud, Firoz Kabir, Bushra Rauf, Fareeha Fatima, et al. 2016. “Deletion at the GCNT2 Locus Causes Autosomal Recessive Congenital Cataracts.” PLoS ONE 11 (12): 1–14. doi:10.1371/journal.pone.0167562.