1. M. Sharma, J. C. Mueller, A. Zimprich, P. Lichtner, A. Hofer, P. Leitner, S. Maass, D. Berg, A. Durr, V. Bonifati, G. De Michele, B. Oostra, A. Brice, N. W. Wood, B. Muller-Myhsok, and T. Gasser. The sepiapterin reductase gene region reveals association in the PARK3 locus: analysis of familial and sporadic Parkinson's disease in European populations. J Med Genet, 43(7):557-62, 2006. Note: European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)Journal ArticleResearch Support, Non-U.S. Gov'tEngland. [WWW] Keyword(s): Age of Onset, Alcohol Oxidoreductases/*genetics, Chromosome Mapping, Genetic Markers, Germany/epidemiology, Humans, Lod Score, Parkinson Disease/*genetics, Parkinsonian Disorders/*genetics, Polymorphism, Genetic, Polymorphism, Single Nucleotide, Reference Values, Siblings.



2. J. Prestel, M. Sharma, P. Leitner, A. Zimprich, J. R. Vaughan, A. Durr, V. Bonifati, G. De Michele, H. A. Hanagasi, M. Farrer, A. Hofer, F. Asmus, G. Volpe, G. Meco, A. Brice, N. W. Wood, B. Muller-Myhsok, and T. Gasser. PARK11 is not linked with Parkinson's disease in European families. Eur J Hum Genet, 13(2):193-7, 2005. Note: European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD)P01 ns40256/ns/nindsJournal ArticleResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.EnglandEjhg. [WWW] Keyword(s): Chromosomes, Human, Pair 2/*genetics, Europe, European Continental Ancestry Group, Humans, *Lod Score, Parkinson Disease/*genetics.



3. A. Abel, N. Fonknechten, A. Hofer, A. Durr, C. Cruaud, T. Voit, J. Weissenbach, A. Brice, S. Klimpe, G. Auburger, and J. Hazan. Early onset autosomal dominant spastic paraplegia caused by novel mutations in SPG3A. Neurogenetics, 5(4):239-43, 2004. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Adolescent, Adult, Age of Onset, Amino Acid Sequence, Child, Exons, Family Health, Female, France, GTP Phosphohydrolases/*genetics, Genes, Dominant, Germany, Humans, Male, Molecular Sequence Data, *Mutation, Missense, Spastic Paraplegia, Hereditary/*genetics.

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