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Detection of neurophysiological features in female R255X MeCP2 mutation mice
Rett syndrome (RTT) is a severe neurodevelopmental disorder (NDD) that is nearly always caused by loss of function mutations in Methyl-CpG-binding Protein 2 (MECP2) and shares many clinical features with other NDD. Genetic restoration of Mecp2 in symptomatic mice lacking MeCP2 expression can reverse...
Gorde:
| Argitaratua izan da: | Neurobiol Dis |
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| Egile Nagusiak: | , , , , , |
| Formatua: | Artigo |
| Hizkuntza: | Inglês |
| Argitaratua: |
2020
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| Gaiak: | |
| Sarrera elektronikoa: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7572861/ https://ncbi.nlm.nih.gov/pubmed/32927061 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2020.105083 |
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