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Posts Tagged ‘Genetic mutations’

Research Advancements Offer Hope for LCA & Usher Syndrome Patients

Leber congenital amaurosis type 10 (LCA10) and Usher syndrome are both genetic diseases that lead to blindness. LCA10 is a retinal disease that leads to severe visual impairment or blindness in early childhood. Usher syndrome is the leading cause of both blindness and deafness, with type 2A (USH2A) being the most common type. This type […]