Long-term human IgG treatment improves heart and muscle function in a mouse model of Duchenne muscular dystrophy.

Fibrotic replacement was also reduced after treatment with IgG, but the difference did not quite reach statistical significance ( P = 0.0574) ( Figure 3 E–G). 3.4 Ex vivo muscle contraction test and serum CK levels Diaphragm segments of IgG‐treated animals were less susceptible to fatigue.

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