Cite
A new heterozygous mutation in the stop codon of CRYAB (p.X176Y) is liable for congenital posterior pole cataract in a Chinese family.
MLA
Yu, Yinhui, et al. “A New Heterozygous Mutation in the Stop Codon of CRYAB (p.X176Y) Is Liable for Congenital Posterior Pole Cataract in a Chinese Family.” Ophthalmic Genetics, vol. 42, no. 2, Apr. 2021, pp. 139–43. EBSCOhost, https://doi.org/10.1080/13816810.2020.1855665.
APA
Yu, Y., Xu, J., Qiao, Y., Li, J., & Yao, K. (2021). A new heterozygous mutation in the stop codon of CRYAB (p.X176Y) is liable for congenital posterior pole cataract in a Chinese family. In Ophthalmic Genetics (Vol. 42, Issue 2, pp. 139–143). https://doi.org/10.1080/13816810.2020.1855665
Chicago
Yu, Yinhui, Jingjie Xu, Yue Qiao, Jinyu Li, and Ke Yao. 2021. “A New Heterozygous Mutation in the Stop Codon of CRYAB (p.X176Y) Is Liable for Congenital Posterior Pole Cataract in a Chinese Family.” Ophthalmic Genetics. Vol. 42. doi:10.1080/13816810.2020.1855665.