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. Author manuscript; available in PMC: 2014 Feb 1.
Published in final edited form as: Circ Cardiovasc Genet. 2013 Feb;6(1):118–131. doi: 10.1161/CIRCGENETICS.110.959387

Figure 6.

Figure 6

The cardiac sarcomere, highlighting protein products of genes involved in hypertrophic cardiomyopathy. Disease-causing variants in cardiac myosin-binding protein C (MYBPC3) and beta-myosin heavy chain (MYH7) are most common, accounting for 20-45% and 15-20% of the disease respectively. Cardiac troponin T type 2 (TNNT2) and troponin I type 3 (TNNI3) each account for ~5%. Variation in other sarcomere genes is less frequent. Data from Ackerman et al.36