Dated: Jun 01, 2022
Publication Name: International Journal of Biological Macromolecules
Citations : TAT-MeCP2 protein variants rescue disease phenotypes in human and mouse models of Rett syndrome
Rett syndrome (RTT) is a neurodevelopmental disorder caused by pathogenic variants leading to functional impairment of the MeCP2 protein.
Contributors: Hannes Steinkellner, Prakasha Kempaiah, Alexander V.Beribisky, Sandra Pferschy, Julia Etzler, AnnaHuber, Victoria Sarne, Winfried Neuhaus, Mario Kuttke, Jan Bauer, Jayamuruga P. Arunachalam, John Christodoulou, Ralf Dressel, Alexander Mildner, Marco Prinz, Franco Laccone