Autosomal Dominant Optic Atrophy (ADOA) is a hereditary form of blindness, in which the most common cause is a mutation in Opa1, a protein involved in the fusion of the inner mitochondrial membrane…
Autosomal Dominant Optic Atrophy (ADOA) is the most common form of congenital neuropathy and caused primarily by mutations in the gene coding for the mitochondrial membrane-remodeling enzyme Opa1…