Article: Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of
2022 Volume 16, Page(s) 823060
Abstract: 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- ... ...
Abstract | 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 |
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Language | English |
Publishing date | 2022-02-15 |
Publishing country | Switzerland |
Document type | Journal Article |
ZDB-ID | 2411902-7 |
ISSN | 1662-453X ; 1662-4548 |
ISSN (online) | 1662-453X |
ISSN | 1662-4548 |
DOI | 10.3389/fnins.2022.823060 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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