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Rare Insights

Exploring the ideas, innovations, and individuals shaping the future of rare disease.

From family to framework: how SLC6A1 Connect UK-AQ is reshaping collaboration in rare epilepsy

September 10, 2025 | 2:29 pm

When Lindsay Randall’s son Arthur was diagnosed in 2018 with SLC6A1 Developmental and Epileptic Encephalopathy, there were[…]

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RAREready™ – structured EU JCA readiness for rare-disease sponsors

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