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Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease, affecting approximately 1 percent of the population over age 50. Recent studies have confirmed significant familial aggregation of PD and a large number of large multicase families have been documented. Genetic markers on chromosome 4q21-q23 were found to be linked to the PD phenotype in a large kindred with autosomal dominant PD, with a Z max = 6.00 for marker D4S2380 . This finding will facilitate identification of the gene and research on the pathogenesis of PD.
Genetic Markers, Male, Phenotype, Genetic Linkage, Chromosome Mapping, Humans, Female, Parkinson Disease, Chromosomes, Human, Pair 4, Lod Score, Pedigree
Genetic Markers, Male, Phenotype, Genetic Linkage, Chromosome Mapping, Humans, Female, Parkinson Disease, Chromosomes, Human, Pair 4, Lod Score, Pedigree
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 733 | |
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| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 0.1% |
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