A natural history study of autosomal dominant GUCY2D-associated cone –rod dystrophy

ConclusionWe have described the natural long-term decline in vision and cone function associated with mutations in GUCY2D and identified a set of functional and structural biomarkers that may be useful as outcome parameters for future therapeutic clinical trials.
Source: Documenta Ophthalmologica - Category: Opthalmology Source Type: research