Clinical Trial Update: Universal Rare Gene Study: A Registry and Natural History Study of Retinal Dystrophies Associated With Rare Disease-Causing Genetic Variants

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Summary

A registry and natural history study investigating retinal dystrophies associated with rare disease-causing genetic variants; currently recruiting participants.

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Diseases / indications

• Inherited Retinal Degeneration
• Retinitis Pigmentosa

Snippet

Sponsor: Jaeb Center for Health Research | Conditions: Inherited Retinal Degeneration, Retinitis Pigmentosa | Status: RECRUITING