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Rett Syndrome and MeCP2
Rett syndrome (RTT) is a severe and progressive neurological disorder, which mainly affects young females. Mutations of the methyl-CpG binding protein 2 (MECP2) gene are the most prevalent cause of classical RTT cases. MECP2 mutations or altered expression are also associated with a spectrum of neur...
Tallennettuna:
| Julkaisussa: | Neuromolecular Med |
|---|---|
| Päätekijät: | , |
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5798978/ https://ncbi.nlm.nih.gov/pubmed/24615633 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12017-014-8295-9 |
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