The Diagnostic Journey of a Patient with Prader-Willi-Like Syndrome and a Unique Homozygous <i>SNURF-SNRPN</i> Variant; Bio-Molecular Analysis and Review of the Literature.

However, whereas overexpression of SNRPN-WT showed a small trend in reducing neuronal maturation (Neurite length: One-Way ANOVA: F[2,45] = 6.29, p = 0.003; SNRPN-WT versus empty vector control: p = 0.0627, Tukey’s multiple comparison test; Arborization: One-Way ANOVA: F[2,45] = 5.66, p = 0.006; SNRPN-WT versus empty vector control: p = 0.44, Tukey’s multiple com

also in 722 other papers