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The origin of genetic instability in CCTG repeats
CCTG tetranucleotide repeat expansion is associated with a hereditary neurological disease called myotonic dystrophy type 2 (DM2). The underlying reasons that lead to genetic instability and thus repeat expansion during DNA replication remains elusive. Here, we have shown CCTG repeats have a high pr...
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| Main Authors: | , , , |
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| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
Oxford University Press
2011
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3152338/ https://ncbi.nlm.nih.gov/pubmed/21478167 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr185 |
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