Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia.

MLA

Erjavec, Elisa, et al. “Congenital Microcoria Deletion in Mouse Links Sox21 Dysregulation to Disease and Suggests a Role for TGFB2 in Glaucoma and Myopia.” American Journal of Human Genetics, vol. 111, no. 10, Oct. 2024, pp. 2265–82. EBSCOhost, https://doi.org/10.1016/j.ajhg.2024.08.019.

APA

Erjavec, E., Angée, C., Hadjadj, D., Passet, B., David, P., Kostic, C., Dodé, E., Zanlonghi, X., Cagnard, N., Nedelec, B., Crippa, S. V., Bole-Feysot, C., Zarhrate, M., Creuzet, S., Castille, J., Vilotte, J.-L., Calvas, P., Plaisancié, J., Chassaing, N., & Kaplan, J. (2024). Congenital microcoria deletion in mouse links Sox21 dysregulation to disease and suggests a role for TGFB2 in glaucoma and myopia. American Journal of Human Genetics, 111(10), 2265–2282. https://doi.org/10.1016/j.ajhg.2024.08.019

Chicago

Erjavec, Elisa, Clémentine Angée, Djihad Hadjadj, Bruno Passet, Pierre David, Corinne Kostic, Emmanuel Dodé, et al. 2024. “Congenital Microcoria Deletion in Mouse Links Sox21 Dysregulation to Disease and Suggests a Role for TGFB2 in Glaucoma and Myopia.” American Journal of Human Genetics 111 (10): 2265–82. doi:10.1016/j.ajhg.2024.08.019.