@inproceedings{inproceedings, title = {{De novo variants in the non-coding spliceosomal snRNA gene RNU4-2 are a frequent cause of syndromic neurodevelopmental disorders}}, url = {{}}, year = {{2024}}, month = {{12}}, author = {{Chen Y and Dawes R and Kim HC and Stenton S and Walker S and Ljungdahl A and Lord J and Ganesh VS and Ma J and Martin-Geary A and Lemire G et al}}, volume = {{32}}, journal = {{EUROPEAN JOURNAL OF HUMAN GENETICS}}, pages = {{854-854}}, note = {{Accessed on 2026/01/25}}}