Myotilinopathy: refining the clinical and myopathological phenotype
Author:
Publisher
Oxford University Press (OUP)
Subject
Neurology (clinical)
Link
http://academic.oup.com/brain/article-pdf/128/10/2315/768780/awh576.pdf
Reference24 articles.
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2. Ferreiro A, Ceuterick-de Groote Ch, Marks JJ, Goemans N, Schreiber G, Hanefeld F, et al. Desmin-related myopathy with Mallory body-like inclusions is caused by mutations of the selenoprotein N gene. Ann Neurol2004; 55: 676–86.
3. Ferrer I, Martín B, Castaño JG, Lucas JJ, Moreno D, Olive M. Proteasomal expression and activity, and induction of the immunoprotesome in myofibrillar myopathies and inclusion body myositis. J Neuropathol Exp Neurol2004; 63: 484–98.
4. Ferrer I, Carmona M, Blanco R, Moreno D, Torrejón-Escribano B, Olivé M. Involvement of clusterin and the aggresome in abnormal protein deposits in myofibrillar myopathies and inclusion body myositis. Brain Pathol2005; 15: 101–8.
5. Freixes M, Puig B, Rodríguez A, Torrejon-Escribano B, Blanco R, Ferrer I. Clusterin solubility and aggregation in Creutzfeldt-Jakob disease. Acta Neuropathol2004; 108: 295–301.
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