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. 2010 Jul;51(7):3340–3346. doi: 10.1167/iovs.09-4659

Figure 4.

Figure 4.

Level of the m.3243A>G point mutation in single muscle fibers dissected from the EOM and skeletal muscle (SKM) of patient 13. The m.3243G>A mutation was nearly homoplasmic in COX-deficient EOM and skeletal muscle fibers, with no significant difference in the threshold of COX deficiency in these two muscle groups (P = 0.2).