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The dystrophin-associated protein complex (DAPC) is an assembly of proteins that links the extracellular matrix (ECM), sarcolemma and actin cytoskeleton in skeletal and cardiac muscle. Mutations in its components are linked to a variety of muscle disorders, including Duchenne muscular dystrophy, and this reflects its critical role in preservation of muscle integrity. In Cell Science at a Glance on p. 2801, Kay Davies and co-workers provide a model of the DAPC, surveying its main components and the diseases with which they are associated.
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