piRNAs Warrant Investigation in Rett Syndrome: An Omics Perspective
Mutations in the MECP2 gene are found in a large proportion of girls with Rett Syndrome. Despite extensive research, the principal role of MeCP2 protein remains elusive. Is MeCP2 a regulator of genes, acting in concert with co-activators and co-repressors, predominantly as an activator of target gen...
| Main Authors: | , , |
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| Format: | Online |
| Language: | English |
| Published: |
IOS Press
2012
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| Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3810717/ |