Sheck, L., Davies, W. I., Moradi, P., Robson, A. G., Kumaran, N., Liasis, A. C., . . . Michaelides, M. (2018). Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies. Ophthalmology, 125(6), 894-903. https://doi.org/10.1016/j.ophtha.2017.12.013

Sheck, Leo, Wayne I.L Davies, Phillip Moradi, Anthony G. Robson, Neruban Kumaran, Alki C. Liasis, Andrew R. Webster, Anthony T. Moore, and Michel Michaelides. "Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies." Ophthalmology 125, no. 6 (2018): 894-903. https://doi.org/10.1016/j.ophtha.2017.12.013.

Sheck, Leo, et al. "Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies." Ophthalmology, vol. 125, no. 6, 2018, pp. 894-903, https://doi.org/10.1016/j.ophtha.2017.12.013.