Long‐term human IgG treatment improves heart and muscle function in a mouse model of Duchenne muscular dystrophy
Abstract Background Duchenne muscular dystrophy (DMD) is a progressive muscle‐wasting disease caused by mutations in the dystrophin gene, which leads to structural instability of the dystrophin-glycoprotein‐complex with subsequent muscle degeneration. In addition, muscle inflammation has been implic...
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Main Authors: | , , , , , , , , |
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Format: | Book |
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Wiley,
2020-08-01T00:00:00Z.
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A1234.567 |
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