Corticobasal syndrome and primary progressive aphasia as manifestations of LRRK2 gene mutations. [electronic resource]
Producer: 20080306Description: 521-7 p. digitalISSN:- 1526-632X
- Adult
- Aged
- Aged, 80 and over
- Aphasia, Primary Progressive -- genetics
- Brain -- pathology
- DNA Mutational Analysis
- Female
- Genetic Markers -- genetics
- Genetic Predisposition to Disease -- genetics
- Genetic Testing
- Genotype
- Heredodegenerative Disorders, Nervous System -- genetics
- Humans
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Male
- Middle Aged
- Mutation -- genetics
- Phenotype
- Predictive Value of Tests
- Protein Serine-Threonine Kinases -- genetics
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Publication Type: Journal Article; Research Support, N.I.H., Extramural
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