Načítá se...
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...
Uloženo v:
| Vydáno v: | Neuromolecular Med |
|---|---|
| Hlavní autoři: | , |
| Médium: | Artigo |
| Jazyk: | Inglês |
| Vydáno: |
2014
|
| Témata: | |
| On-line přístup: | 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 |
| Tagy: |
Přidat tag
Žádné tagy, Buďte první, kdo otaguje tento záznam!
|