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Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy

โœ Scribed by Nicoletta Checcarelli; Allessandro Prelle; Maurizio Moggio; Giacomo Comi; Nereo Bresolin; Alex Papadimitriou; Gigliola Fagiolari; Andreina Bordoni; Guglielmo Scarlato


Book ID
118932070
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
726 KB
Volume
123
Category
Article
ISSN
0022-510X

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## Abstract Inclusion body myositis, a chronic inflammatory disorder, is the most common cause of myopathy in adults over the age of 50. Diagnosis is based on clinical features and distinctive morphological findings by both light and electron microscopy. The causes of inclusion body myositis are st