Corticobasal syndrome and primary progressive aphasia as manifestations of lrrk2 gene mutations. [electronic resource]
Producer: 20080902Description: 303; author reply 303-4 p. digitalISSN:- 1526-632X
- Aphasia, Primary Progressive -- genetics
- Causality
- DNA Mutational Analysis -- standards
- Genetic Markers -- genetics
- Genetic Predisposition to Disease -- genetics
- Genetic Testing -- standards
- Genetic Variation -- genetics
- Genotype
- Humans
- Inheritance Patterns -- genetics
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Mutation -- genetics
- Neurodegenerative Diseases -- genetics
- Norway
- Parkinson Disease -- genetics
- Protein Serine-Threonine Kinases -- genetics
- Risk Factors
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Publication Type: Letter; Comment
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