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Insulin Signaling as a Key Moderator in Myotonic Dystrophy Type 1
Myotonic dystrophy type 1 (DM1) is an autosomal dominant genetic disease characterized by multi-system involvement. Affected organ system includes skeletal muscle, heart, gastro-intestinal system and the brain. In this review, we evaluate the evidence for alterations in insulin signaling and their r...
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| 出版年: | Front Neurol |
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| 主要な著者: | , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Frontiers Media S.A.
2019
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6901991/ https://ncbi.nlm.nih.gov/pubmed/31849810 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2019.01229 |
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