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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: Jana Zschüntzsch (Author), Pia Vanessa Jouvenal (Author), Yaxin Zhang (Author), Florian Klinker (Author), Malte Tiburcy (Author), David Liebetanz (Author), Dörthe Malzahn (Author), Heinrich Brinkmeier (Author), Jens Schmidt (Author)
Format: Book
Published: Wiley, 2020-08-01T00:00:00Z.
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