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...
Veröffentlicht in: | Neural plasticity. - 1998. - 2012(2012) vom: 28., Seite 104796 |
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Format: | Online-Aufsatz |
Sprache: | English |
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2012
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Zugriff auf das übergeordnete Werk: | Neural plasticity |
Schlagworte: | Journal Article Review FMR1 protein, human MicroRNAs Fragile X Mental Retardation Protein 139135-51-6 |
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