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Myotonic Dystrophies: Targeting Therapies for Multisystem Disease
Myotonic dystrophy is an autosomal dominant muscular dystrophy not only associated with muscle weakness, atrophy, and myotonia but also prominent multisystem involvement. There are 2 similar, but distinct, forms of myotonic dystrophy; type 1 is caused by a CTG repeat expansion in the DMPK gene, and...
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| 出版年: | Neurotherapeutics |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Springer International Publishing
2018
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6277298/ https://ncbi.nlm.nih.gov/pubmed/30341596 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13311-018-00679-z |
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