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