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CTG-Repeat Detection in Primary Human Myoblasts of Myotonic Dystrophy Type 1
Myotonic dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder caused by unstable CTG-repeat expansions in the DMPK gene. Tissue mosaicism has been described for the length of these repeat expansions. The most obvious affected tissue is skeletal muscle, making it the first target fo...
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| 出版年: | Front Neurosci |
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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.
2021
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8274452/ https://ncbi.nlm.nih.gov/pubmed/34262431 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnins.2021.686735 |
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