Exome Sequencing Identifies Three Novel Candidate Genes Implicated in Intellectual Disability
Figure 3
The sequencing chromatograms of the families MRQ14, MRQ11 and MRQ15.
(A) Shows the panels containing the region with the identified KMT2B mutation in family MRQ14: ancestral (left panel), heterozygous (middle panel) and variant (right panel) (B) shows the region containing the identified ZNF589 mutation in family MRQ11: ancestral (left panel), heterozygous (middle panel) and variant (right panel). (C) shows the de novo variant of HHAT in family MRQ15: ancestral (left panel), heterozygous (right panel).
