LCA5 抗体
(Leber Congenital Amaurosis 5 (LCA5))
This gene encodes a protein that is thought to be involved in centrosomal or ciliary functions. Mutations in this gene cause Leber congenital amaurosis type V. Alternatively spliced transcript variants are described. [provided by RefSeq, Oct 2009].
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Latest Publications for our LCA5 抗体
: "Identification of a novel splice-site mutation in the Lebercilin (LCA5) gene causing Leber congenital amaurosis." in: Molecular vision, Vol. 14, pp. 481-6, (2008) (PubMed).
Aliases for LCA5 抗体
LCA5, lebercilin (LCA5) 抗体Leber congenital amaurosis 5 (LOC787523) 抗体
LCA5, lebercilin (Lca5) 抗体
Leber congenital amaurosis 5 (human) (Lca5) 抗体
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5730406O13Rik 抗体
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