Dystonia musculorum (dt J /dt J ) mutant mice suffer from a degeneration of spinocerebellar tracts as well as a dystrophy of peripheral sensory tracts. This neurological mutant has been proposed as an animal model of human cerebellar ataxia, in particular of the Friedreich's type; thus, it was deeme
β¦ LIBER β¦
Essential conservation of D1mutant phenotype at the level of individual topographies of behaviour in mice lacking both D1and D3dopamine receptors
β Scribed by John Y. F. Wong; Jeremiah J. Clifford; Jim S. Massalas; Anthony Kinsella; John L. Waddington; John Drago
- Publisher
- Springer
- Year
- 2003
- Tongue
- English
- Weight
- 220 KB
- Volume
- 167
- Category
- Article
- ISSN
- 0033-3158
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