Two-year progression analysis of RPE65 autosomal dominant retinitis pigmentosa.

CONCLUSION: adRP due to a mutation in the gene encoding RPE65 phenocopied choroideremia. Based on our analysis of the 2-year disease progression in this patient, RPE65 adRP is mild and has a slow rate of disease progression. PMID: 29947567 [PubMed - in process]

https://www.ncbi.nlm.nih.gov/pubmed/29947567?dopt=Abstract

Source: Ophthalmic Genetics - June 28, 2018 Category: Opthalmology Tags: Ophthalmic Genet Source Type: research