Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleMice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.AuthorsYasui, Dag H.; Gonzales, Michael L.; Aflatooni, Justin O.; Crary, Florence K.; Hu, Daniel J.; Gavino, Bryant J.; Golub, Mari S.; Vincent, John B.; Schanen, N. Carolyn; Olson, Carl O.; Rastegar, Mojgan; Lasalle, Janine M.PublicationHuman Molecular Genetics, 2014, Vol 23, Issue 24, p6695ISSN0964-6906Publication typeArticleDOI10.1093/hmg/ddu496