Mice with an isoform-ablating Mecp2exon 1 mutation recapitulate the neurologic deficits of Rett syndrome

Dag H. Yasui, Michael L. Gonzales, Justin O. Aflatooni, Florence K. Crary, Daniel J. Hu, Bryant J. Gavino, Mari S. Golub, John B. Vincent, N. Carolyn Schanen, Carl O. Olson, Mojgan Rastegar, Janine M LaSalle

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