Clinical Research Details A Natural History and Outcome Measure Discovery Study of PRPF31 Mutation–Associated Retinal Dystrophy (20226317) Study Description A Natural History and Outcome Measure Discovery Study of PRPF31 Mutation–Associated Retinitis Pigmentosa Inclusion/Exclusion Criteria Patients with Retinitis Pigmentosa with PRPF31 Gene mutations will be screened Open Enrollment Contact Name: Ghulam HamdaniContact Phone: (904) 244-9347Contact Email: ghulam.hamdani@jax.ufl.edu Investigators Sandeep Grover, M.D. Ophthalmology