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Home > Our Research Activities > List Of Publications > Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases

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Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Correction: Solving unsolved rare neurological diseases-a Solve-RD viewpoint

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