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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
- Correspondence to: Professor A Clarke Institute of Medical Genetics, Cardiff University, University Hospital of Wales, Cardiff CF14 4XN, UK; clarkeaj{at}cf.ac.uk
Citation
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
Publication history
- Received July 7, 2006
- Accepted July 12, 2006
- Revised July 7, 2006
- First published August 11, 2006.
Online issue publication
February 09, 2007
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- Previous version (11 August 2006).
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Copyright 2007 Journal of Medical Genetics