Retinal dystrophy associated with a single-base deletion mutation in mitochondrial DNA 3271 in patient with MELAS syndrome

ConclusionsThese findings indicate that the RPE atrophy was wider and the rod dysfunction was more severe affected than that of previously reported MELAS cases with the m.3243A  >  G mutation.

Source: Documenta Ophthalmologica - January 30, 2019 Category: Opthalmology Source Type: research