A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity

Figure 3

The pedigree of the examined family, the proband is marked by arrow. He is the only clinically affected (black symbol), + indicates family members who are heterozygous for the p.V79I mutation, − indicates family members who were genetically assessed and found to be nonmutation carriers. The three family members with borderline HCM are marked by a black quadrant. SB: still birth. SD marks a 19-year-old girl who suddenly died. No further information was available as to the cause of death.