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InsightRP2 What's new
Here you’ll find current topics, events, and news about our research
Our review article published in Human Mutation presents current knowledge on RP2-associated retinopathy and highlights gaps and unmet needs.
Our article in Human Gene Therapy presents InsightRP2, our integrated, multimodal research network on RP2-associated retinopathy.
Mutations in the RP2 gene cause a specific form of the inherited retinal disease retinitis pigmentosa. The InsightRP2 registry helps clinicians and researchers better understand the genetic basis and disease progression of RP2-associated retinitis pigmentosa ...