Fig. 1From: Targeted massively parallel sequencing of autism spectrum disorder-associated genes in a case control cohort reveals rare loss-of-function risk variantsSanger sequencing of the loss-of-function de novo variant in RBFOX1. The patient in whom the RBFOX1 premature stop variant was identified along with parents, and three unaffected siblings were sequenced using standard Sanger capillary sequencing. The ASD patient has a C/T genotype (N) while all other family members are C/C Back to article page