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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