Sangeetha Kandoi

No ORCID on file · 1 paper in corpus · active 2023
2023
Disease modeling and pharmacological rescue of autosomal dominant Retinitis Pigmentosa associated with RHO copy number variation
·doi:10.1101/2023.02.27.23286248

Retinitis pigmentosa (RP), a heterogenous group of inherited retinal disorder causes slow progressive vision loss with no effective treatments available. Mutations in the rhodopsin gene ( RHO ), account for ∼25% cases of autosomal dominant…