M. Bonyadi

Genetic Insights Into Retinitis Pigmentosa: A De Novo RPGR Mutation in an Iranian–Azeri Family

Retinitis pigmentosa (RP) is a genetically heterogeneous disease characterized by progressive vision loss and blindness, primarily due to the degeneration of cone photoreceptor cells. The classic symptoms include a decline in visual acuity and retinal atrophy. In this study, whole‐exome sequencing (WES) was performed o...