Abstract
Leber congenital amaurosis (LCA) is an early severe form of retinal dystrophy. Mutations in at least 18 genes cause LCA, including crumbs homolog 1 (CRB1), which may account for 10% of LCA.
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Schedule a callMore From: Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus
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