reference/31740858

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endingPage	903
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bibliographicCitation	Sheck L, Davies WIL, Moradi P, Robson AG, Kumaran N, Liasis AC, Webster AR, Moore AT, Michaelides M. Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies. Ophthalmology. 2018 Jun;125(6):894–903. doi: 10.1016/j.ophtha.2017.12.013.
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date	201806
identifier	https://pubmed.ncbi.nlm.nih.gov/29398085 https://doi.org/10.1016/j.ophtha.2017.12.013 https://pubmed.ncbi.nlm.nih.gov/PMC5974693
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Leber Congenital Amaurosis Associated with Mutations in CEP290, Clinical Phenotype, and Natural History in Preparation for Trials of Novel Therapies
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