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2. S. Lesage, L. Leclere, E. Lohmann, M. Borg, M. Ruberg, A. Durr, and A. Brice. Frequency of the LRRK2 G2019S mutation in siblings with Parkinson's disease. Neurodegener Dis, 4(2-3):195-8, 2007. Note: French Parkinson's Disease Genetics Study GroupNs41723-01a1/ns/nindsJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tSwitzerland. [WWW]



3. P. Ibanez, S. Lesage, E. Lohmann, S. Thobois, G. De Michele, M. Borg, Y. Agid, A. Durr, and A. Brice. Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa. Brain, 129(Pt 3):686-94, 2006. Note: French Parkinson's Disease Genetics Study GroupNs41723-01a1/ns/nindsCase ReportsJournal ArticleMulticenter StudyResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tEnglanda journal of neurology. [WWW] Keyword(s): Adult, Age of Onset, Aged, Amino Acid Sequence, DNA Mutational Analysis, Female, Humans, Male, Middle Aged, Molecular Sequence Data, *Mutation, Parkinsonian Disorders/*genetics, Pedigree, Protein Kinases/*genetics, Sequence Alignment, Ubiquitin-Protein Ligases/genetics.

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