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pubmed-article:7747013pubmed:abstractTextA 52-year-old man had a cardiomyopathy for 22 years as had his brother. Both required pacemakers. For the past 12 years, he also suffered from increasing muscle weakness. His muscle fibres contained granulo-filamentous material as previously seen in muscle fibres of a French family with myopathy and cardiomyopathy. It was rich in desmin, alpha-B crystallin, and dystrophin, the connotation, pathogenesis, and common denominator of which, however, remain unexplained.lld:pubmed
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pubmed-article:7747013pubmed:articleTitleImmunohistologic and electron microscopic abnormalities of desmin and dystrophin in familial cardiomyopathy and myopathy.lld:pubmed
pubmed-article:7747013pubmed:affiliationDivision of Neuropathology, Johannes-Gutenberg University, Mainz/Germany.lld:pubmed
pubmed-article:7747013pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7747013pubmed:publicationTypeCase Reportslld:pubmed
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