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LCA5
Lebercilin, also known as leber congenital amaurosis 5 (LCA5), is a protein that in humans is encoded by the ''LCA5'' gene.〔(【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=167691 )〕 This protein is thought to be involved in centrosomal or ciliary functions. == Clinical significance ==
Mutations in the ''LCA5'' gene are associated with Leber's congenital amaurosis.
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「LCA5」の詳細全文を読む
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