CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy typ...
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I
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Publisher
England: BioMed Central
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Language
English
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Publisher
England: BioMed Central
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Contents
Myotonic Dystrophy type I (DM1) is the most common muscular dystrophy in adults. Previous reports have highlighted that neuromuscular junctions (NMJs) deteriorate in skeletal muscle from DM1 patients and mouse models thereof. However, the underlying pathomechanisms and their contribution to muscle dysfunction remain unknown.
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Full title
CaMKIIβ deregulation contributes to neuromuscular junction destabilization in Myotonic Dystrophy type I
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TN_cdi_doaj_primary_oai_doaj_org_article_af7b40e3a50f4837b9d4e0a855e85038
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https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_af7b40e3a50f4837b9d4e0a855e85038
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ISSN
2044-5040
E-ISSN
2044-5040
DOI
10.1186/s13395-024-00345-3
