Prospective Open Clinical and Genetic Study of Patients With Retinitis Pigmentosa

Conditions:   Retinitis Pigmentosa;   Usher Syndromes Intervention:   Diagnostic Test: Whole Exome Sequencing Sponsors:   Sensor Technology for Deafblind;   Central Clinical Hospital under President Affairs;   Deaf-Blind Support Foundation Con-nection;   Federal State Budgetary Institution Moscow Helmholtz Eye Research Institute;   Federal State Budgetary Institution Research Center for Medical Genet ics;   Oftalmic LLC;   Center for Genetics and Reproductive Medicine Genetico Enrolling by invitation
Source: ClinicalTrials.gov - Category: Research Source Type: clinical trials