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Neurotrophic effects of Cerebrolysin in the Mecp2308/Ytransgenic model of Rett syndrome

✍ Scribed by Edith Doppler; Edward Rockenstein; Kiren Ubhi; Chandra Inglis; Michael Mante; Anthony Adame; Leslie Crews; Monika Hitzl; Herbert Moessler; Eliezer Masliah

Book ID
106073693
Publisher
Springer-Verlag
Year
2008
Tongue
English
Weight
940 KB
Volume
116
Category
Article
ISSN
0001-6322

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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