ConteXt of change—X inactivation and disease
Author:
Affiliation:
1. Research Institute of Molecular Pathology, Vienna, Austria
2. Present address: Wellcome Trust Centre for Stem Cell Research, Cambridge, UK
Publisher
EMBO
Subject
Molecular Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/emmm.200900053
Reference85 articles.
1. SATB1 Defines the Developmental Context for Gene Silencing by Xist in Lymphoma and Embryonic Cells
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2
3. Severe phenotype of chronic granulomatous disease presenting in a female with a de novo mutation in gp91-phox and a non familial, extremely skewed X chromosome inactivation
4. 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
5. Fragile X Syndrome: Loss of Local mRNA Regulation Alters Synaptic Development and Function
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