Literature DB >> 12913211

Strong association of the Saitohin gene Q7 variant with progressive supranuclear palsy.

R de Silva1, A Hope, A Pittman, M E Weale, H R Morris, N W Wood, A J Lees.   

Abstract

Recent reports are inconclusive in showing that the Q7R polymorphism of the novel Saitohin gene, nested in intron 9 of the tau gene, is associated with AD. The authors show that this polymorphism is in complete linkage disequilibrium with the extended tau H1/H2 haplotype and that the Q variant and QQ genotype of Q7R are strongly associated with progressive supranuclear palsy, implicating it as a possibly important pathogenic candidate.

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Year:  2003        PMID: 12913211     DOI: 10.1212/01.wnl.0000073140.25533.90

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  8 in total

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2.  Towards a complete resolution of the genetic architecture of disease.

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5.  Association of the MAPT locus with Parkinson's disease.

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6.  Linkage disequilibrium fine mapping and haplotype association analysis of the tau gene in progressive supranuclear palsy and corticobasal degeneration.

Authors:  A M Pittman; A J Myers; P Abou-Sleiman; H C Fung; M Kaleem; L Marlowe; J Duckworth; D Leung; D Williams; L Kilford; N Thomas; C M Morris; D Dickson; N W Wood; J Hardy; A J Lees; R de Silva
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7.  Variation at APOE and STH loci and Alzheimer's disease.

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Review 8.  Meta-analysis of the association between variants in MAPT and neurodegenerative diseases.

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  8 in total

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