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A comparative study of X-inactivation in Rett syndrome probands and control subjects

✍ Scribed by T. Webb; E. Watkiss


Book ID
115091893
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
919 KB
Volume
49
Category
Article
ISSN
0009-9163

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## Abstract Rett syndrome (RTT) is caused by mutations in the X‐linked gene __MECP2__. While patients with RTT show widespread changes in brain function, relatively few studies document changes in brain structure and none examine in detail whether mutations causing more severe clinical phenotypes a