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Natural History of Autosomal Dominant Optic Atrophy (ADOA), Caused by OPA1 Mutation

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Clinical Trial

NCT06140329 Recruiting, Active
Natural History of Autosomal Dominant Optic Atrophy (ADOA), Caused by OPA1 Mutation
Observational
Observational

Disease

Disease type

Uveitis

Patient type

Adult

Children

Inclusion / Exclusion

Opening date

28/02/2024

Closing date

31/03/2026

Inclusion criteria :

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Exclusion criteria :

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Funding

Industry

Members involved

Others investigators

Pr Camiel BOON

Representative

Netherlands

Anterior Segment Rare Eye Diseases (WG4), Genetic Diagnostics (TWG6), National Integration (TWG9), Pediatric Ophthalmology Rare Diseases (WG3), Registries & Epidemiology (TWG7), Research (TWG8), Retinal Rare Eye Diseases (WG1)
Working Group Leader
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ERN EYE member investigating site

HCP : Principal investigators