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Juvenile ARRP and LCA have common mutations
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A sequencing study has shown mutations in common genes in juvenile autosomal recessive retinitis pigmentosa (ARRP) and Leber’s congenital amaurosis (LCA), suggesting that the diseases are closely related and explaining their clinical similarity.
Mutations in the commonest genes causing LCA were found in a panel of unrelated patients with juvenile …
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Copyright 2006 British Journal of Ophthalmology