Article
Ataxic mouse mutants and molecular mechanisms of absence epilepsy.
Human molecular genetics - 1 Jan 1999
Fletcher C F, Frankel W N
Abstract excerpt
Mouse genetic models for common human diseases have been studied for most of the 20th century. Although many polygenic strain differences and spontaneous single gene mutants have been extensively characterized over the years, knowing their innermost secrets ultimately requires the identity of the mutated genes. One group of neurological mutants, detected initially due to cerebellar dysfunction, was identified as...
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