X-Chromosome Inactivation Patterns Are Unbalanced and Affect the Phenotypic Outcome in a Mouse Model of Rett Syndrome
Author:
Publisher
Elsevier BV
Subject
Genetics(clinical),Genetics
Reference44 articles.
1. The X-linked methylated DNA binding protein, Mecp2, is subject to X inactivation in the mouse;Adler;Mamm Genome,1995
2. Influence of mutation type and X chromosome inactivation on Rett syndrome phenotypes;Amir;Ann Neurol,2000
3. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl- CpG-binding protein 2;Amir;Nat Genet,1999
4. Survey of MeCP2 in the Rett syndrome and the non-Rett syndrome brain;Armstrong;J Child Neurol,2003
5. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain;Balmer;Hum Genet,2002
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