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Aberrant myokine signaling in congenital myotonic dystrophy
Myotonic dystrophy types 1 (DM1) and 2 (DM2) are dominantly-inherited neuromuscular disorders caused by a toxic gain-of-function of expanded CUG and CCUG repeats, respectively. Although both disorders are clinically similar, congenital myotonic dystrophy (CDM), a severe DM form, is only found in DM1...
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| Publicado no: | Cell Rep |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5689469/ https://ncbi.nlm.nih.gov/pubmed/29091763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.celrep.2017.10.018 |
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