Transcriptomic and Epigenomic Landscape in Rett Syndrome

Transcriptomic and Epigenomic Landscape in Rett Syndrome

Rett syndrome (RTT) is an extremely invalidating, cureless, developmental disorder, and it is considered one of the leading causes of intellectual disability in female individuals. The vast majority of RTT cases are caused by de novo mutations in the X-linked Methyl-CpG binding protein 2 (<i>M...

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Bibliographic Details
Main Authors: Domenico Marano, Salvatore Fioriniello, Maurizio D’Esposito, Floriana Della Ragione
Format: Article
Language:English
Published: MDPI AG 2021-06-01
Series:Biomolecules
Subjects:
Rett syndrome
<i>MeCP2</i>
DNA methylation
epigenomics
non-coding RNAs
transcriptomics
Online Access:https://www.mdpi.com/2218-273X/11/7/967

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https://www.mdpi.com/2218-273X/11/7/967

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