It included four genes: (1) Epilepsy, progressive myoclonus type 2, Laforin disease [laforin] (EPM2A); (2) Uncharacterized protein (RP11-54515.3); (3) SNF2 histone linker PHD RING helicase E3 ubiquitin protein ligase (SHPRH) and (4) F-box protein 30 (FBXO30) as shown in Figure 6b. Here, EPM2A is linked to epilepsy.