Dystonia musculorum (dt) mutant mice, characterized by degeneration of
spinocerebellar tracts, were impaired in terms of horizontal and vert
ical motor activity, hole poking, exploration, and motor coordination.
In tests of motor coordination, their deficits were more severe than
those of previously tested mutant mice with degeneration of cerebellar
cells. However, unlike other cerebellar mutants, dt mutants alternate
d above chance levels in a two-trial spontaneous alternation test, whi
ch is a test of inhibitory tendencies and spatial orientation, and so
dt mutants may not be impaired in these functions.