Targeting OPA1 protein for therapeutic intervention in autosomal dominant optic atrophy: In silico drug discovery
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Autosomal dominant hereditary optic atrophy (ADOA) is a prevalent hereditary condition characterized by the gradual and simultaneous deterioration of vision. Mutations in Optic atrophy 1 (OPA1) have been linked to ADOA, the prevailing form of inherited optic n... ...
