A comparative analysis between patient-derived PBMCs and those from HDs reveals a distinct set of DEGs associated with neurologic disorders, including SNHG5, SLC35F1, RASGEF1B, SLC26A3, LINGO1, SLC27A4, and FAM118A. These findings offer novel insights into the prediction of neurologic changes induced by WD. This evidence concerns the gene RASGEF1B and nervous system disorder.