Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1.

MLA

Prokudin, Ivan, et al. “Exome Sequencing in Developmental Eye Disease Leads to Identification of Causal Variants in GJA8, CRYGC, PAX6 and CYP1B1.” European Journal of Human Genetics, vol. 22, no. 7, July 2014, pp. 907–15. EBSCOhost, https://doi.org/10.1038/ejhg.2013.268.

APA

Prokudin, I., Simons, C., Grigg, J. R., Storen, R., Kumar, V., Phua, Z. Y., Smith, J., Flaherty, M., Davila, S., & Jamieson, R. V. (2014). Exome sequencing in developmental eye disease leads to identification of causal variants in GJA8, CRYGC, PAX6 and CYP1B1. European Journal of Human Genetics, 22(7), 907–915. https://doi.org/10.1038/ejhg.2013.268

Chicago

Prokudin, Ivan, Cas Simons, John R Grigg, Rebecca Storen, Vikrant Kumar, Zai Y Phua, James Smith, Maree Flaherty, Sonia Davila, and Robyn V Jamieson. 2014. “Exome Sequencing in Developmental Eye Disease Leads to Identification of Causal Variants in GJA8, CRYGC, PAX6 and CYP1B1.” European Journal of Human Genetics 22 (7): 907–15. doi:10.1038/ejhg.2013.268.