Rett syndrome mutation MeCP2 T158A disrupts DNA binding, protein stability and ERP responses.

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Published in Nat Neurosci on November 27, 2011

Authors

Darren Goffin1, Megan Allen, Le Zhang, Maria Amorim, I-Ting Judy Wang, Arith-Ruth S Reyes, Amy Mercado-Berton, Caroline Ong, Sonia Cohen, Linda Hu, Julie A Blendy, Gregory C Carlson, Steve J Siegel, Michael E Greenberg, Zhaolan Zhou

Author Affiliations

1: Department of Genetics, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania, USA.

Associated clinical trials:

Rare Diseases Clinical Research Network: Neurophysiological Correlates | NCT03077308

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