Unusual structures of CCTG repeats and their participation in repeat expansion
CCTG repeat expansion in intron 1 of the cellular nucleic acid-binding protein (CNBP) gene has been identified to be the genetic cause of myotonic dystrophy type 2 (DM2). Yet the underlying reasons for the genetic instability in CCTG repeats remain elusive. In recent years, CCTG repeats have been fo...
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| Hlavní autoři: | , |
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| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
De Gruyter
2016-12-01
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| Edice: | Biomolecular Concepts |
| Témata: | |
| On-line přístup: | https://doi.org/10.1515/bmc-2016-0024 |
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