MOLECULAR ANALYSIS OF INDONESIAN LCA PATIENTS AND IN VITRO SPLICE CORRECTION FOR CEP290-ASSOCIATED LCA

Background: Leber congenital amaurosis (LCA) is an autosomal recessive retinal disorder, characterized by an early-onset visual loss, amaurotic pupils, and retinal degeneration. Only a few studies have been described about Indonesian LCA patients. Pre-clinical studies have shown that antisense oligo...

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Main Author: Nugraha, Widya Eka (Author)
Format: Academic Paper
Published: 2015.
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Online Access:http://eprints.undip.ac.id/46670/
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