Fig. 2From: Chromatin remodeling dysfunction extends the etiological spectrum of schizophrenia: a case reportRepresentation of CHD2 variant adapted from the DECIPHER browser. The heterozygous transition in CHD2 (NM_001271.3: c.4003G > T) is predicted to produce a premature stop codon, p.(Glu1335*), which likely brings on non-mediated decay (NMD) so that no protein could be producedBack to article page