Identifying key underlying regulatory networks and predicting targets of orphan C/D box SNORD116 snoRNAs in Prader-Willi syndrome
Nucleic Acids Res. 2024 Nov 22:gkae1129. doi: 10.1093/nar/gkae1129. Online ahead of print. ABSTRACT Prader-Willi syndrome (PWS) is a rare neurodevelopmental disorder characterized by neonatal hypotonia, …