Registries, Research, Events, • 3/4/25 Rare-X Registry - Official Launch (English) Previous Global Community You Might Also Like Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin Dr Nicky Whiffin - The discovery of ReNU syndrome: an overview Research Summit 2025: Dr Nicky Whiffin N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies
Registries, Research, Events, • 3/4/25 Rare-X Registry - Official Launch (English) Previous Global Community You Might Also Like Dr Sarah Wynn - How the discovery of ReNU syndrome is impacting patients and families De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin Dr Nicky Whiffin - The discovery of ReNU syndrome: an overview Research Summit 2025: Dr Nicky Whiffin N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies