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Mechanism of Repeat-Associated MicroRNAs in Fragile X Syndrome
The majority of the human genome is comprised of non-coding DNA, which frequently contains redundant microsatellite-like trinucleotide repeats. Many of these trinucleotide repeats are involved in triplet repeat expansion diseases (TREDs) such as fragile X syndrome (FXS). After transcription, the tri...
Gorde:
| Egile Nagusiak: | , , |
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| Formatua: | Artigo |
| Hizkuntza: | Inglês |
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Hindawi Publishing Corporation
2012
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3388308/ https://ncbi.nlm.nih.gov/pubmed/22779005 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2012/104796 |
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