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Histological study in the brain of thereelin/Dab1-compound mutant mouse

✍ Scribed by Tatsuro Yamamoto; Tomiyoshi Setsu; Ayako Okuyama-Yamamoto; Toshio Terashima


Book ID
107666235
Publisher
Springer Japan
Year
2009
Tongue
English
Weight
891 KB
Volume
84
Category
Article
ISSN
1447-6959

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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