Figure 6
From: SHROOM3 is a novel candidate for heterotaxy identified by whole exome sequencing
Non-synonymous rare variants identified in SHROOM3 mutation screening in heterotaxy patients. Partial SHROOM3 chromatogram showing homozygous rare variants in samples from LAT0820 and LAT0990 and heterozygous variants in LAT0844 and LAT0982. Arrows indicate position of nucleotide changes.