Presence of spinocerebellar ataxia type 2 gene mutation in a patient with apparently sporadic Parkinson's disease: clinical implications. [electronic resource]
Producer: 20050214Description: 1357-60 p. digitalISSN:- 0885-3185
- Aged
- Alleles
- Antiparkinson Agents -- therapeutic use
- Ataxins
- Caudate Nucleus -- diagnostic imaging
- DNA Mutational Analysis
- Dominance, Cerebral -- physiology
- Genetic Carrier Screening
- Genetic Testing
- Humans
- Levodopa -- therapeutic use
- Male
- Middle Aged
- Nerve Tissue Proteins
- Neurologic Examination
- Parkinson Disease -- diagnostic imaging
- Polymerase Chain Reaction
- Positron-Emission Tomography
- Proteins -- genetics
- Putamen -- diagnostic imaging
- Spinocerebellar Ataxias -- diagnostic imaging
- Treatment Outcome
- Trinucleotide Repeats
- Ubiquitin-Protein Ligases -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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