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Several rodent models with spontaneous mutations causing cerebellar pathology are impaired in motor functions during the neonatal period, including Grid2 Lc , Rora sg , Dab1 scm , Girk2 Wv , Lmx1a dr-sst , Myo5a dn , Inpp4a wbl , and Cacna1a rol mice as well as shaker and dystonic rats. Deficits are also evident in murine null mutants...
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