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Leber Congenital Amaurosis 10
A Leber congenital amaurosis that is characterized by severe infantile-onset cone-rod dystrophy with high hyperopia and severe ERG abnormalities and is caused by mutation in the CEP290 gene on chromosome 12q21.32.
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Overview
A Leber congenital amaurosis that is characterized by severe infantile-onset cone-rod dystrophy with high hyperopia and severe ERG abnormalities and is caused by mutation in the CEP290 gene on chromosome 12q21.32.
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