Exome Sequencing Identifies Three Novel Candidate Genes Implicated in Intellectual Disability
Figure 1
Pedigree of families (A) MRQ14, (B) MRQ11 and (C) MRQ15.
The segregation of mutation of KMT2B, ZNF589 and HHAT are also in the pedigree. The symbol +/+ represents homozygous ancestral alleles, M/M is for homozygous variant alleles and +/M is for heterozygous carriers. In the panel B, the genotype of the father (III:1) has been deduced.
