Identification of molecular signatures and pathways involved in Rett syndrome using a multi-omics approach
Abstract Background Rett syndrome (RTT) is a neurodevelopmental disorder mainly caused by mutations in the methyl-CpG-binding protein 2 gene (MECP2). MeCP2 is a multi-functional protein involved in many cellular processes, but the mechanisms by which its dysfunction causes disease are not fully unde...
Furkejuvvon:
| Váldodahkkit: | , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
BMC
2023-09-01
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| Ráidu: | Human Genomics |
| Fáttát: | |
| Liŋkkat: | https://doi.org/10.1186/s40246-023-00532-1 |
| Fáddágilkorat: |
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