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MeCP2 Deficiency Leads to Loss of Glial Kir4.1
Rett syndrome (RTT) is an X-linked neurodevelopmental disorder usually caused by mutations in methyl-CpG-binding protein 2 (MeCP2). RTT is typified by apparently normal development until 6–18 mo of age, when motor and communicative skills regress and hand stereotypies, autonomic symptoms, and seizur...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | eNeuro |
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| Κύριοι συγγραφείς: | , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Society for Neuroscience
2018
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5818552/ https://ncbi.nlm.nih.gov/pubmed/29464197 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/ENEURO.0194-17.2018 |
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