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...

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Bibliographische Detailangaben
Veröffentlicht in:Neural plasticity. - 1998. - 2012(2012) vom: 28., Seite 104796
1. Verfasser: Kelley, Karen (VerfasserIn)
Weitere Verfasser: Chang, Shin-Ju E, Lin, Shi-Lung
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2012
Zugriff auf das übergeordnete Werk:Neural plasticity
Schlagworte:Journal Article Review FMR1 protein, human MicroRNAs Fragile X Mental Retardation Protein 139135-51-6