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Mitochondrial abnormalities in the Mecp2tm1Tam mouse model of Rett syndrome

✍ Scribed by S.L. Williamson; W.A. Gold; G.J. Pelka; P.P.L. Tam; J. Gibson; J. Christodoulou⁎


Book ID
116752179
Publisher
Elsevier Science
Year
2011
Tongue
English
Weight
86 KB
Volume
11
Category
Article
ISSN
1567-7249

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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