CNVs disrupt several genes associated with SCZ, including TBX1 (also associated with autism), ERBB4 (encodes a receptor for NDF/heregulin), SLC1A3 (a glutamate transporter), RAPGEF4 (a nucleotide exchange factor), and CIT (a neuronal Rho-target gene) [7,8]. The gene discussed is NRG1; the disease is autism.