Depletion of rabphilin 3A in a transgenic mouse model (R6/1) of Huntington's disease, a possible culprit in synaptic dysfunction
Keywords: Huntington's disease; R6/1; Mouse; Synapse; Synaptic dysfunction; Exocytosis; Huntingtin; Vesicle protein; CAG repeat; Neurodegeneration; Polyglutamine; Rabphilin;