LCA5
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Lua error in Module:Infobox_gene at line 53: attempt to index field 'wikibase' (a nil value). Lebercilin, also known as leber congenital amaurosis 5 (LCA5), is a protein that in humans is encoded by the LCA5 gene.[1][2][3] This protein is thought to be involved in centrosomal or ciliary functions.
Clinical significance
[edit | edit source]Mutations in the LCA5 gene are associated with Leber's congenital amaurosis.
References
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