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

<table>A homology analysis of the known MYL3 mutations, the valine in residue 79 is highly conserved.</table>

Biochemistry Research International

Figure 4: A Novel Myosin Essential Light Chain Mutation Causes Hypertrophic Cardiomyopathy with Late Onset and Low Expressivity 