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
✦ LIBER ✦
Dopamine D1 and D2 receptors in progressive supranuclear palsy: An autoradiographic study
✍ Scribed by Dr. J. Pascual; J. Berciano; B. Grijalba; E del Olmo; A. M. González; J. Figols; A. Pazos
- Publisher
- John Wiley and Sons
- Year
- 1992
- Tongue
- English
- Weight
- 623 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0364-5134
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