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Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy

Human Molecular Genetics · 1999 · Vol. 8(4) · pp. 711–715
Mary V. BakerIrene LitvanHenry HouldenJoy AdamsonDennis W. DicksonJordi Pérez‐TurJohn HardyTimothy LynchEileen H. BigioM. Hutton

Abstract

We describe two extended haplotypes that cover the human tau gene. In a total of approximately 200 unrelated caucasian individuals there is complete disequilibrium between polymorphisms which span the gene (which covers approximately 100 kb of DNA). This suggests that the establishment of the two haplotypes was an ancient event and either that recombination is suppressed in this region, or that recombinant genes are selected against. Furthermore, we show that the more common haplotype (H1) is significantly over-represented in patients with progressive supranuclear palsy (PSP), extending earlier reports of an association between an intronic dinucleotide polymorphism and PSP.

Alzheimer's disease research and treatmentsParkinson's Disease Mechanisms and TreatmentsRNA regulation and diseaseHaplotypeProgressive supranuclear palsyBiologyGeneticsLinkage disequilibriumGeneAlleleDisequilibriumAtrophy

MeSH terms

AgedAllelesDNA Mutational AnalysisExonsGene FrequencyGenotypeHaplotypesHumansMiddle AgedPolymorphism, GeneticSupranuclear Palsy, Progressivetau Proteins
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Cited by
Neurodegenerative Tauopathies
Annual Review of Neuroscience · 2001 · 2,357 citations
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