The enhancement of activity rescues the establishment of Mecp2 null neuronal phenotypes

MECP2 mutations cause Rett syndrome (RTT), a severe and progressive neurodevelopmental disorder mainly affecting females. Although RTT patients exhibit delayed onset of symptoms, several evidences demonstrate that MeCP2 deficiency alters early development of the brain. Indeed, during early maturatio...

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Udgivet i:EMBO Mol Med
Main Authors: Scaramuzza, Linda, De Rocco, Giuseppina, Desiato, Genni, Cobolli Gigli, Clementina, Chiacchiaretta, Martina, Mirabella, Filippo, Pozzi, Davide, De Simone, Marco, Conforti, Paola, Pagani, Massimiliano, Benfenati, Fabio, Cesca, Fabrizia, Bedogni, Francesco, Landsberger, Nicoletta
Format: Artigo
Sprog:Inglês
Udgivet: John Wiley and Sons Inc. 2021
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Articles
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC8033520/
https://ncbi.nlm.nih.gov/pubmed/33665914
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15252/emmm.202012433
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