Among the DE genes, fourteen candidate genes for WS were identified for the first time: CEPBD, METTL21EP, DUSP8, NELL2, UBE3D, PDK4, DDIT4, FKBP5, DGAT2, LIPG, TDH, RGCC, COL4A5, and COL4A6. This evidence concerns the gene NELL2 and Werner syndrome.