Frequency of the D620N mutation in VPS35 in Parkinson disease. [electronic resource]
Producer: 20130311Description: 1360-4 p. digitalISSN:- 1538-3687
- Aged
- Chile
- Cognition Disorders -- etiology
- Family Health
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Genetic Testing
- Genotype
- Germany
- Humans
- Longitudinal Studies
- Male
- Middle Aged
- Mutation -- genetics
- Parkinson Disease -- complications
- Serbia
- Tertiary Care Centers
- United States
- Vesicular Transport Proteins -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't
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