A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.

MLA

Micheal, Shazia, et al. “A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.” PloS One, vol. 11, no. 7, July 2016, p. e0160016. EBSCOhost, https://doi.org/10.1371/journal.pone.0160016.

APA

Micheal, S., Siddiqui, S. N., Zafar, S. N., Villanueva-Mendoza, C., Cortés-González, V., Khan, M. I., & den Hollander, A. I. (2016). A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma. PloS One, 11(7), e0160016. https://doi.org/10.1371/journal.pone.0160016

Chicago

Micheal, Shazia, Sorath Noorani Siddiqui, Saemah Nuzhat Zafar, Cristina Villanueva-Mendoza, Vianney Cortés-González, Muhammad Imran Khan, and Anneke I den Hollander. 2016. “A Novel Homozygous Mutation in FOXC1 Causes Axenfeld Rieger Syndrome with Congenital Glaucoma.” PloS One 11 (7): e0160016. doi:10.1371/journal.pone.0160016.