Fig. 3From: Whole-exome sequencing and homozygosity mapping identify variants in NCOR1 and MAP2K3 associated with non-syndromic congenital heart defectsa Structural organization of NCOR1 in CHD cases with three nonsynonymous damaging variants: G207C, C241T, and G244A. b Structural organization of MAP2K3 with three nonsynonymous variants: G194T, C199T, and C578TBack to article page