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. 2015 Jul 8;2:15023. doi: 10.1038/mtm.2015.23

Figure 2.

Figure 2

Disease-specific change of Pompe disease iPSCs. (a) Mutation analysis shows compound heterozygote mutation (c.796 C>A and c.1316 T>A). (b) Electron microscopy of iPS cell lines (Pompe-1, Pompe2, Pompe3, and control). Arrow is demonstrating accumulated glycogen. Upper scale bar, 5 µm; lower scale bar, 1 µm. (c) GAA enzyme assay of iPS cell lines (Control, Pompe1, Pompe2, and Pompe3). Data were expressed as means ± SEM. (d) Glycogen assay of iPS cell lines (Control, Pompe1, Pompe2, and Pompe3). Data were expressed as means ± SEM.