Fig. 1
From: Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders
Familial segregation of selected monoallelic rare variants identified by WGS. Individuals II-2 and III-1 have multiple diagnoses including ASD. Individual I-1 was coded as likely affected with a major psychiatric disorder and/or NDD. See text for details. A female paternal first cousin of the proband (not pictured), with possible persistent depressive disorder and no suspected NDD, did not carry the 15q21 deletion or the GRIK5 missense variant