Identification of Region-Specific Cytoskeletal and Molecular Alterations in Astrocytes of Mecp2 Deficient Animals
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DOI: 10.3389/fnins.2022.823060
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-linked MECP2 gene, coding for the methyl-CpG-binding protein 2… read more here.
Keywords: alterations astrocytes; mecp2 deficient; molecular alterations; mecp2 deficiency ... See more keywords