Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations. [electronic resource]
Producer: 20061018Description: 1250-4 p. digitalISSN:- 0003-9942
- Aged
- DNA Mutational Analysis -- methods
- Family Health
- Female
- Gene Frequency
- Genetic Predisposition to Disease
- Glycine -- genetics
- Humans
- Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
- Male
- Middle Aged
- Mutation
- Parkinson Disease -- epidemiology
- Protein Serine-Threonine Kinases -- genetics
- Serine -- genetics
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Publication Type: Comparative Study; Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.
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