9/1/25

RNU2-2 Mutations Cause Severe Neurodevelopmental Disorder with Epilepsy

🧠 The study uncovers recurrent de novo variants and sheds light on how disruptions in major spliceosomal snRNAs can drive disease—expanding our understanding of spliceopathies beyond previously known syndromes like ReNU Syndrome.

🔍 A must-listen for anyone interested in RNA biology, genomic medicine, and the molecular basis of brain disorders.