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    A broad phenotypic screen identifies novel phenotypes driven by a single mutant allele in Huntington’s Disease CAG knock-in mice by Hölter-Koch, Sabine (Author) , Stromberg, Mary (Author) , Kovalenko, Marina (Author) , Garrett, Lillian (Author) , Glasl, Lisa (Author) , Lopez, Edith (Author) , Guide, Jolene (Author) , Götz, Alexander (Author) , Hans, Wolfgang (Author) , Becker, Lore (Author) , Rathkolb, Birgit (Author) , Rozman, Jan (Author) , Schrewe, Anja (Author) , Klingenspor, Martin (Author) , Klopstock, Thomas (Author) , Schulz, Holger (Author) , Wolf, Eckhard (Author) , Wursta, Wolfgang (Author) , Gillis, Tammy (Author) , Wakimoto, Hiroko (Author) , Seidman, Jonathan (Author) , MacDonald, Marcy E. (Author) , Cotman, Susan (Author) , Gailus-Durner, Valérie (Author) , Fuchs, Helmut (Author) , Angelis, Martin Hrabě de (Author) , Lee, Jong-Min (Author) , Wheeler, Vanessa C. (Author) ,


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