Intravitreal delivery of a novel AAV vector targets ON bipolar cells and restores visual function in a mouse model of complete congenital stationary night blindnessMiranda L. Scalabrino, Sanford L. Boye(University of Florida)Human Molecular GeneticsAugust 26, 201510.1093/hmg/ddv341Cited by 73SaveCiteExport RISWatch citationsRelated PapersSARM1 depletion rescues NMNAT1-dependent photoreceptor cell death and retinal degeneration|eLife|2020|81