Personal Stories, • 10/21/25 Italian News segment features RNU4-2 / ReNU syndrome families Previous Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families Next Sibling Superheroes You Might Also Like N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin 2025 ReNU Hope Conference ReNU Syndrome 🧬 – RNU4-2 Mutations and Neurodevelopmental Disorders In conversation with James Coney and Shaun Pye, a webinar for Rare Chromo Day 2025
Personal Stories, • 10/21/25 Italian News segment features RNU4-2 / ReNU syndrome families Previous Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families Next Sibling Superheroes You Might Also Like N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin 2025 ReNU Hope Conference ReNU Syndrome 🧬 – RNU4-2 Mutations and Neurodevelopmental Disorders In conversation with James Coney and Shaun Pye, a webinar for Rare Chromo Day 2025
