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Publications of M. Farrer
Articles in journal or book chapters
  1. Y. Baba, Y. Tsuboi, M. C. Baker, R. J. Uitti, M. L. Hutton, D. W. Dickson, M. Farrer, J. D. Putzke, B. K. Woodruff, B. Ghetti, J. R. Murrell, B. F. Boeve, R. C. Petersen, P. Verpillat, A. Brice, M. B. Delisle, O. Rascol, K. Arima, M. W. Dysken, M. Yasuda, T. Kobayashi, N. Sunohara, O. Komure, S. Kuno, A. D. Sperfeld, G. Stoppe, J. Kohlhase, S. Pickering-Brown, D. Neary, O. Bugiani, and Z. K. Wszolek. The effect of tau genotype on clinical features in FTDP-17. Parkinsonism Relat Disord, 11(4):205-8, 2005. Note: Journal ArticleEngland. [WWW] Keyword(s): Adult, Age of Onset, Dementia/*genetics, Female, Genotype, Humans, Male, Microtubule-Associated Proteins/*genetics, Middle Aged, Parkinsonian Disorders/*genetics, Phenotype, tau Proteins/*genetics.


  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. N. Rawal, M. Periquet, E. Lohmann, C. B. Lucking, H. A. Teive, G. Ambrosio, S. Raskin, S. Lincoln, N. Hattori, J. Guimaraes, M. W. Horstink, W. Dos Santos Bele, E. Brousolle, A. Destee, Y. Mizuno, M. Farrer, J. F. Deleuze, G. De Michele, Y. Agid, A. Durr, and A. Brice. New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism. Neurology, 60(8):1378-81, 2003. Note: French Parkinson's Disease Genetics Study GroupEuropean Consortium on Genetic Susceptibility in Parkinson's Disease1 r01 ns41723â\texteuro``01a1/ns/nindsJournal ArticleResearch Support, Non-U.S. Gov'tResearch Support, U.S. Gov't, P.H.S.United States. [WWW] Keyword(s): Adult, Codon, Nonsense, DNA Mutational Analysis, Exons/genetics, Female, Genes, Recessive, Humans, Male, Middle Aged, Phenotype, Point Mutation, Polymerase Chain Reaction, RNA Splice Sites/genetics, Ubiquitin-Protein Ligases/*genetics.



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