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TWEAK/Fn14, a pathway and novel therapeutic target in myotonic dystrophy
Myotonic dystrophy type 1 (DM1), the most prevalent muscular dystrophy in adults, is characterized by progressive muscle wasting and multi-systemic complications. DM1 is the prototype for disorders caused by RNA toxicity. Currently, no therapies exist. Here, we identify that fibroblast growth factor...
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| Publicat a: | Hum Mol Genet |
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| Autors principals: | , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Oxford University Press
2015
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| Matèries: | |
| Accés en línia: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4355029/ https://ncbi.nlm.nih.gov/pubmed/25504044 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddu617 |
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