Molecular signatures of inherited and acquired sporadic late onset nemaline myopathies
Molecular signatures of inherited and acquired sporadic late onset nemaline myopathies
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Publisher
England: BioMed Central Ltd
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Language
English
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Publisher
England: BioMed Central Ltd
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Contents
Acquired sporadic late onset nemaline myopathy (SLONM) and inherited nemaline myopathy (iNM) both feature accumulation of nemaline rods in muscle fibers. Unlike iNM, SLONM is amenable to therapy. The distinction between these disorders is therefore crucial when the diagnosis remains ambiguous after initial investigations. We sought to identify biom...
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Full title
Molecular signatures of inherited and acquired sporadic late onset nemaline myopathies
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TN_cdi_doaj_primary_oai_doaj_org_article_6acd5dccc2d54faeb9ba149869c3f6dd
Permalink
https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_6acd5dccc2d54faeb9ba149869c3f6dd
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ISSN
2051-5960
E-ISSN
2051-5960
DOI
10.1186/s40478-023-01518-9
