Mecp2 deficiency leads to delayed maturation and altered gene expression in hippocampal neurons
Author:
Publisher
Elsevier BV
Subject
Neurology
Reference67 articles.
1. Unbiased characterization of high-density oligonucleotide microarrays using probe-level statistics;Aimone;J. Neurosci. Methods,2004
2. Spatial and temporal gene expression profiling of the contused rat spinal cord;Aimone;Exp. Neurol.,2004
3. Expression pattern of the Rett syndrome gene MeCP2 in primate prefrontal cortex;Akbarian;Neurobiol. Dis.,2001
4. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat. Genet.,1999
5. Neuropathology of Rett syndrome;Armstrong;Ment. Retard. Dev. Disabil. Res. Rev.,2002
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