Affiliation: Stanford University
- Ube3a expression is not altered in Mecp2 mutant miceCharandle Jordan
Department of Genetics, Stanford University School of Medicine, CA 94305 5323, USA
Hum Mol Genet 15:2210-5. 2006..We, therefore, challenge the conclusion that decreased UBE3A/Ube3a expression contributes to the pathophysiology of RTT...
- Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targetsCharandle Jordan
Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305 5323, USA
BMC Med Genet 8:36. 2007..Most mutations occur de novo during spermatogenesis. Located at Xq28, MECP2 is subject to X inactivation, and affected females are mosaic. Rare hemizygous males suffer from a severe congenital encephalopathy...