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Dive into the research topics of 'Mice with an isoform-ablating Mecp2exon 1 mutation recapitulate the neurologic deficits of Rett syndrome'. Together they form a unique fingerprint.- Sort by
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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
Research output: Contribution to journal › Article › peer-review