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A low absolute number of expanded transcripts is involved in myotonic dystrophy type 1 manifestation in muscle
Muscular manifestation of myotonic dystrophy type 1 (DM1), a common inheritable degenerative multisystem disorder, is mainly caused by expression of RNA from a (CTG·CAG)(n)-expanded DM1 locus. Here, we report on comparative profiling of expression of normal and expanded endogenous or transgenic tran...
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| 出版年: | Hum Mol Genet |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Oxford University Press
2016
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4805313/ https://ncbi.nlm.nih.gov/pubmed/26908607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddw042 |
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