Multiple-system atrophy is genetically distinct from identified inherited causes of spinocerebellar degeneration. [electronic resource]
Producer: 19980116Description: 1598-604 p. digitalISSN:- 0028-3878
- Alleles
- Animals
- Ciliary Neurotrophic Factor
- Genotype
- Heterozygote
- Homozygote
- Humans
- Insulin-Like Growth Factor I -- metabolism
- Mice
- Mice, Neurologic Mutants -- genetics
- Multiple System Atrophy -- genetics
- Mutation
- Nerve Tissue Proteins -- genetics
- Receptors, Somatomedin -- genetics
- Repetitive Sequences, Nucleic Acid
- Sequence Homology, Nucleic Acid
- Spinocerebellar Degenerations -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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