Comparative study of brain morphology inMecp2mutant mouse models of Rett syndrome
Author:
Publisher
Wiley
Subject
General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1002/cne.21673/fullpdf
Reference45 articles.
1. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
2. Correlation between clinical severity in patients with Rett syndrome with a p. R168X or p.T158M MECP2 mutation, and the direction and degree of skewing of X-chromosome inactivation;Archer;J Med Genet,2007
3. The neuropathology of the Rett syndrome;Armstrong;Brain Dev,1992
4. Neuropathology of Rett syndrome;Armstrong;Ment Retard Dev Disabil Res Rev,2002
5. Selective dendritic alterations in the cortex of Rett syndrome;Armstrong;J Neuropathol Exp Neurol,1995
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