SERCA1 and calsequestrin storage myopathy: A new surplus protein myopathy

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Abstract

We describe four patients, from four different families, affected by a mild myopathy or asymptomatic elevated serum creatine kinase levels, in whom toluidine blue-stained semithin sections of muscle specimens revealed inclusions of different size and shape. The inclusions did not stain by routine histochemical studies. The sarcoplasmic or endoplasmic reticulum calcium 1 (SERCA1) ATPase and/or calsequestrin reactivity of inclusions, by immunohistochemistry, and the SERCA1- and calsequestrin-increased expression, by immunoblot, suggested that inclusions were constituted by an excess of proteins normally present in the terminal cisternae of sarcoplasmic reticulum. Our cases, both sporadic and familial, represent a new type of surplus protein myopathy. © The Author (2006). Published by Oxford University Press on behalf of the Guarantors of Brain. All rights reserved.

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Tomelleri, G., Palmucci, L., Tonin, P., Mongini, T., Marini, M., L’Erario, R., … Vattemi, G. (2006). SERCA1 and calsequestrin storage myopathy: A new surplus protein myopathy. Brain, 129(8), 2085–2092. https://doi.org/10.1093/brain/awl128

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