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Repeat instability during DNA repair: Insights from model systems
The expansion of repeated sequences is the cause of over 30 inherited genetic diseases, including Huntington disease, myotonic dystrophy (types 1 and 2), fragile X syndrome, many spinocerebellar ataxias, and some cases of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD). Repeat...
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| 出版年: | Crit Rev Biochem Mol Biol |
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| 主要な著者: | , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2015
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4454471/ https://ncbi.nlm.nih.gov/pubmed/25608779 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3109/10409238.2014.999192 |
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