Retinitis pigmentosa (RP) refers to disorders characterized by degeneration of photoreceptors in the eye, which hinders visual ability by absence of photoactivated electrical signals in retina, and nontransmission of those signals to the visual cortex [1][2][3][4] The prevalence of RP is ~80,000 patients in the US, out of which 20,000 patients have vision 20/200 or less. RP is most often inherited as an autosomal recessive trait with large number of cases having this form of inheritance. 1,5 Further, vision loss increases with ageing, 6 which is a major concern since our population is living longer. Current clinical treatments are primarily focussed on slowing down disease