Subcellular partitioning of Nhlh2 mRNA reveals how SNORD116 loss contributes to Prader-Willi Syndrome.
Shadi Ariyanfar, Matthew Adam Kocher, Christopher K. Thompson, Stuart A. Tobet, Deborah J. Good
The paper shows that Snord116 regulates Nhlh2 mRNA localization, with loss of Snord116 causing cytoplasmic Nhlh2 mRNA in hypothalamic neurons, impacting Prader-Willi Syndrome.
bioRxiv · Jan 23, 2026 · PreprintNeuroscience