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2. M. Martinez, A. Brice, J. R. Vaughan, A. Zimprich, M. M. Breteler, G. Meco, A. Filla, M. J. Farrer, C. Betard, A. Singleton, J. Hardy, G. De Michele, V. Bonifati, B. A. Oostra, T. Gasser, N. W. Wood, and A. Durr. Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease. Am J Med Genet B Neuropsychiatr Genet, 136(1):72-4, 2005. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited Statesthe official publication of the International Society of Psychiatric Genetics. [WWW] Keyword(s): Alleles, Apolipoprotein E4, Apolipoproteins E/*genetics, Chromosomes, Human, Pair 19/*genetics, Family Health, Gene Frequency, Genotype, Humans, *Linkage (Genetics), Linkage Disequilibrium, Lod Score, Microsatellite Repeats, Parkinson Disease/*genetics, Siblings.



3. V. Bonifati, P. Rizzu, M. J. van Baren, O. Schaap, G. J. Breedveld, E. Krieger, M. C. Dekker, F. Squitieri, P. Ibanez, M. Joosse, J. W. van Dongen, N. Vanacore, J. C. van Swieten, A. Brice, G. Meco, C. M. van Duijn, B. A. Oostra, and P. Heutink. Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism. Science, 299(5604):256-9, 2003. Note: Journal ArticleResearch Support, Non-U.S. Gov'tUnited States. [WWW] Keyword(s): Alleles, Amino Acid Sequence, Amino Acid Substitution, Animals, Base Sequence, Brain/metabolism, COS Cells, Cell Nucleus/metabolism, Chromosomes, Human, Pair 1, Cloning, Molecular, Cytoplasm/metabolism, DNA, Complementary, Exons, Genes, Recessive, Humans, Intracellular Signaling Peptides and Proteins, Molecular Sequence Data, *Mutation, Oncogene Proteins/chemistry/*genetics/metabolism, Oxidative Stress, PC12 Cells, Parkinsonian Disorders/*genetics/metabolism, Pedigree, Physical Chromosome Mapping, Point Mutation, Protein Structure, Secondary, Rats, Reverse Transcriptase Polymerase Chain Reaction, Sequence Deletion, Transfection.

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