Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of
MeCP2
Rett syndrome (RTT)
astrocyte
cytoskeleton
heterogeneity
Journal
Frontiers in neuroscience
ISSN: 1662-4548
Titre abrégé: Front Neurosci
Pays: Switzerland
ID NLM: 101478481
Informations de publication
Date de publication:
2022
2022
Historique:
received:
26
11
2021
accepted:
24
01
2022
entrez:
4
3
2022
pubmed:
5
3
2022
medline:
5
3
2022
Statut:
epublish
Résumé
Rett syndrome (RTT) is a neurodevelopmental disorder that represents the most common genetic cause of severe intellectual disability in females. Most patients carry mutations in the X-linked
Identifiants
pubmed: 35242007
doi: 10.3389/fnins.2022.823060
pmc: PMC8886113
doi:
Types de publication
Journal Article
Langues
eng
Pagination
823060Informations de copyright
Copyright © 2022 Albizzati, Florio, Miramondi, Sormonta, Landsberger and Frasca.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The handling editor declared a shared affiliation, though no other collaboration with several of the authors IS and NL at the time of the review.
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