Research, • 10/15/24 IEU Seminar: Andrew Mumford and Daniel Greene Previous De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin Next N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies You Might Also Like 2025 ReNU Hope Conference We Belong Together Rare-X Registry - Official Launch (English) Our Diagnostic Odysseys ReNU Syndrome 🧬 – RNU4-2 Mutations and Neurodevelopmental Disorders
Research, • 10/15/24 IEU Seminar: Andrew Mumford and Daniel Greene Previous De Novo Variants in snRNA RNU4-2 Cause a Frequent Neurodevelopmental Syndrome — Prof Nicola Whiffin Next N.Whiffin - The non-coding exome in rare disease: from diagnosis to therapies You Might Also Like 2025 ReNU Hope Conference We Belong Together Rare-X Registry - Official Launch (English) Our Diagnostic Odysseys ReNU Syndrome 🧬 – RNU4-2 Mutations and Neurodevelopmental Disorders
