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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 (MECP2) gen...
Shranjeno v:
| izdano v: | Biomolecules |
|---|---|
| Main Authors: | , , , |
| Format: | Artigo |
| Jezik: | Inglês |
| Izdano: |
MDPI
2021
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| Teme: | |
| Online dostop: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8301932/ https://ncbi.nlm.nih.gov/pubmed/34209228 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/biom11070967 |
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