Short tandem repeat variants are possibly associated with RNA secondary structure and gene expression.
Short tandem repeats (STRs) are abundant in the human genome with approximately 300,000 embedded in gene introns, exons, and untranslated regions. High penetrance STR variants cause human diseases such as Myotonic dystrophy, Baratela-Scott syndrome, and various ataxias. The possibility that STRs con...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Public Library of Science (PLoS)
2025-01-01
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| Series: | PLoS ONE |
| Online Access: | https://doi.org/10.1371/journal.pone.0326355 |
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