MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome
Annie Vogel Ciernia, Dag H. Yasui, Michael C. Pride, Blythe P Durbin-Johnson, Adriana B Noronha, Alene Chang, Trina A. Knotts, Jennifer M. Rutkowsky, Jon Jay Ramsey, Jacqueline N. Crawley, Janine M. LaSalle
This study shows that MeCP2-e1 mutation in mice reproduces motor and metabolic issues seen in Rett syndrome patients.
Human Molecular Genetics · Aug 17, 2018Peer-reviewedNeuroscience