Alterations of Gene Expression and Glutamate Clearance in Astrocytes Derived from an MeCP2-Null Mouse Model of Rett Syndrome
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Reference43 articles.
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3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2.;RE Amir;Nat Genet,1999
4. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome.;J Guy;Nat Genet,2001
5. Deficiency of methyl-CpG binding protein-2 in CNS neurons results in a Rett-like phenotype in mice.;RZ Chen;Nat Genet,2001
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