Clinical Trial
Disease
Disease type
Hereditary retinal disease
Usher Syndrome
Patient type
Adult
Children
Inclusion / Exclusion
Funding
Public
Members involved
Main investigators
Pr Carel HOYNG
Representative
Netherlands
Genetic Diagnostics (TWG6), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
ERN EYE member investigating site
HCP : Principal investigators
Radboud university medical center, Nijmegen, Netherlands
Adress
Geert Grooteplein Zuid 10
6525 GA Nijmegen
Netherlands