Presentations Category: RDH12
Natural History and Genotype-Phenotype Correlations in RDH12-Associated Retinal Degeneration
Detailed Clinical Characterisation, Unique Features, and Natural History of Autosomal Recessive RDH12-Associated Retinal Degeneration
Development of a Gene Therapy Vector for RDH12-Associated Retinal Dystrophy
RDH12 Mutations Cause a Severe Retinal Degeneration With Relatively Spared Rod Function
Aleman et al., Investigative Ophthalmology and Visual Science 2018