Cerebellar pathophysiology in a mouse model of Duchenne muscular dystrophy
This series of experiments investigated dystrophin localization in the normal cerebellum and examined Purkinje neuron function in normal and dystrophin-deficient mice to better understand the physiological basis for cognitive deficits associated with Duchenne muscular dystrophy (DMD), a common genet...
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2012
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Online Access: | http://hdl.handle.net/1993/11296 |