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Kumaran N, Moore AT, Weleber RG, Michaelides M. Leber congenital amaurosis/early-onset severe retinal dystrophy: clinical features, molecular genetics and therapeutic interventions. Br J Ophthalmol. 2017;101:1147–54.
Sheck L, WIL D, Moradi P, Robson AG, Kumaran N, Liasis AC, et al. Leber congenital amaurosis associated with mutations in CEP290, clinical phenotype, and natural history in preparation for trials of novel therapies. Ophthalmology. 2018;125(6):894–903. https://doi.org/10.1016/j.ophtha.2017.12.013. [Epub ahead of print].
Takkar B, Bansal P, Venkatesh P. Leber’s congenital amaurosis and gene therapy. Indian J Pediatr. 2018;85:237–42.
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Tsang, S.H., Sharma, T. (2018). Leber Congenital Amaurosis. In: Tsang, S., Sharma, T. (eds) Atlas of Inherited Retinal Diseases. Advances in Experimental Medicine and Biology, vol 1085. Springer, Cham. https://doi.org/10.1007/978-3-319-95046-4_26
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DOI: https://doi.org/10.1007/978-3-319-95046-4_26
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