1. E. Guettard, M. F. Portnoi, K. Lohmann-Hedrich, B. Keren, S. Rossignol, S. Winkler, I. El Kamel, S. Leu, E. Apartis, M. Vidailhet, C. Klein, and E. Roze. Myoclonus-dystonia due to maternal uniparental disomy. Arch Neurol, 65(10):1380-5, 2008. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW]



2. D. G. Healy, M. Falchi, S. S. O'Sullivan, V. Bonifati, A. Durr, S. Bressman, A. Brice, J. Aasly, C. P. Zabetian, S. Goldwurm, J. J. Ferreira, E. Tolosa, D. M. Kay, C. Klein, D. R. Williams, C. Marras, A. E. Lang, Z. K. Wszolek, J. Berciano, A. H. Schapira, T. Lynch, K. P. Bhatia, T. Gasser, A. J. Lees, and N. W. Wood. Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study. Lancet Neurol, 7(7):583-90, 2008. Note: International LRRK2 ConsortiumG0400000/United Kingdom Medical Research CouncilK08 NS044138/NS/United States NINDSNS R01-36960/NS/United States NINDSP01AG017216/AG/United States NIAP50NS40256/NS/United States NINDSR01AG015866/AG/United States NIAJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, Non-P.H.S.England. [WWW]



3. L. N. Clark, E. Haamer, H. Mejia-Santana, J. Harris, S. Lesage, A. Durr, S. J. Bs, K. Hedrich, E. D. Louis, L. J. Cote, H. Andrews, S. Fahn, C. Waters, B. Ford, S. Frucht, W. Scott, C. Klein, A. Brice, H. Roomere, R. Ottman, and K. Marder. Construction and validation of a Parkinson's disease mutation genotyping array for the Parkin gene. Mov Disord, 22(7):932-7, 2007. Note: Ns32527/ns/nindsNs36630/ns/nindsNs41723-01a1/ns/nindsRr00645/rr/ncrrJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Family Health, Gene Expression Profiling/*methods, Genetics, Population, Genotype, Humans, *Mutation, Oligonucleotide Array Sequence Analysis/*methods, Parkinson Disease/epidemiology/*genetics, Reproducibility of Results, Retrospective Studies, Ubiquitin-Protein Ligases/*genetics.



4. A. Grunewald, G. J. Breedveld, K. Lohmann-Hedrich, C. F. Rohe, I. R. Konig, J. Hagenah, N. Vanacore, G. Meco, A. Antonini, S. Goldwurm, S. Lesage, A. Durr, F. Binkofski, H. Siebner, A. Munchau, A. Brice, B. A. Oostra, C. Klein, and V. Bonifati. Biological effects of the PINK1 c.1366C>T mutation: implications in Parkinson disease pathogenesis. Neurogenetics, 8(2):103-9, 2007. Note: Journal ArticleUnited States. [WWW]



5. D. Kemlink, O. Polo, P. Montagna, F. Provini, K. Stiasny-Kolster, W. Oertel, A. de Weerd, S. Nevsimalova, K. Sonka, B. Hogl, B. Frauscher, W. Poewe, C. Trenkwalder, P. P. Pramstaller, L. Ferini-Strambi, M. Zucconi, E. Konofal, I. Arnulf, G. M. Hadjigeorgiou, S. Happe, C. Klein, A. Hiller, P. Lichtner, T. Meitinger, B. Muller-Myshok, and J. Winkelmann. Family-based association study of the restless legs syndrome loci 2 and 3 in a European population. Mov Disord, 22(2):207-12, 2007. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesofficial journal of the Movement Disorder Society. [WWW] Keyword(s): Chromosomes, Human, Pair 12/*genetics, Chromosomes, Human, Pair 14/*genetics, Chromosomes, Human, Pair 9/*genetics, Europe/epidemiology, Female, Gene Frequency/genetics, Genetic Markers, *Genotype, Haplotypes, Humans, International Cooperation, Linkage Disequilibrium/genetics, Male, Middle Aged, Polymerase Chain Reaction, Polymorphism, Genetic/genetics, Restless Legs Syndrome/*ethnology/*genetics.

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