Φορτώνει......
Unexpected cellular players in Rett syndrome pathology
Rett syndrome is a devastating neurodevelopmental disorder, primarily caused by mutations of methyl CpG-binding protein 2 (MeCP2). Although the genetic cause of disease was identified over a decade ago, a significant gap still remains in both our clinical and scientific understanding of its pathogen...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Neurobiol Dis |
|---|---|
| Κύριοι συγγραφείς: | , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2015
|
| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4644494/ https://ncbi.nlm.nih.gov/pubmed/25982834 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2015.05.005 |
| Ετικέτες: |
Προσθήκη ετικέτας
Δεν υπάρχουν, Καταχωρήστε ετικέτα πρώτοι!
|