Structural and immunocytochemical features of olivopontocerebellar atrophy caused by the spinocerebellar ataxia type 1 (SCA-1) mutation define a unique phenotype. [electronic resource]
Producer: 19960605Description: 572-81 p. digitalISSN:- 0001-6322
- Adolescent
- Adult
- Atrophy
- Brain -- pathology
- Child
- Chromosome Mapping
- Chromosomes, Human, Pair 6 -- ultrastructure
- Dentate Gyrus -- pathology
- Humans
- Immunohistochemistry
- Middle Aged
- Mutation
- Neural Pathways -- pathology
- Olivopontocerebellar Atrophies -- genetics
- Phenotype
- Red Nucleus -- pathology
- Spinal Cord -- pathology
- Spinocerebellar Degenerations -- genetics
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Publication Type: Journal Article; Research Support, U.S. Gov't, P.H.S.
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