Cytoskeletal derangements in hereditary myopathy with a desmin L345P mutation


Patients with abnormal accumulations of desmin have been described in myopathies with or without cardiac involvement. Desmin deposits were sometimes associated with abnormal aggregates of other cytoskeletal proteins. In the present study we present how the cytoskeletal organisation of desmin, nestin, synemin, paranemin, plectin and αB-crystallin is altered… (More)
DOI: 10.1007/s00401-002-0583-z


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