@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}}}