MECP2 is progressively expressed in post-migratory neurons and is involved in neuronal maturation rather than cell fate decisions
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Cellular and Molecular Neuroscience,Molecular Biology
Reference76 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
2. Neuropathology of Rett syndrome;Armstrong;Ment. Retard. Dev. Disabil. Res. Rev.,2002
3. Selective dendritic alterations in the cortex of Rett syndrome;Armstrong;J. Neuropathol. Exp. Neurol.,1995
4. Microscopic observations of the brain in Rett syndrome;Bauman;Neuropediatrics,1995
5. Pervasive neuroanatomic abnormalities of the brain in three cases of Rett's syndrome;Bauman;Neurology,1995
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