Abstract
LCA5 encodes lebercilin, which is involved in microtubule transport. Mutations in LCA5 cause 1–2% of autosomal recessive Leber congenital amaurosis [1–5].
References
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Zahid, S. et al. (2018). LCA5 . In: Retinal Dystrophy Gene Atlas. Springer, Cham. https://doi.org/10.1007/978-3-319-10867-4_43
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DOI: https://doi.org/10.1007/978-3-319-10867-4_43
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