In agreement with our findings, samples from patients with Focal Cortical Dysplasia, which display many cellular similarities with TSC lesions, contain a small subset of dysmorphic neurons that express VGAT and DLX1 or DLX2 transcription factors expressed by cells derived from the medial ganglionic eminences (Lamparello et al., 2007). The gene discussed is SLC32A1; the disease is Focal cortical dysplasia.