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RAPID: a targeted long-read RNA workflow for functional resolution of splicing variants in rare disease

  • Published on: January 2 2026
  • Source: medRxiv
Authors: Kylie Montgomery, Hannah Macpherson, Claire Anderson, Charles Wade, Emil K Gustavsson, David S Lynch, Louise C Wilson, James Davison, Emma Wakeling, Karin Tuschl, Henry Houlden, Emma Clement, Phillipa Mills, Mina Ryten

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