Linkage disequilibrium fine mapping and haplotype association analysis of the <i>tau</i> gene in progressive supranuclear palsy and corticobasal degeneration

Abstract

The findings support the pathological evidence that underlying variations in MAPT could contribute to disease pathogenesis by subtle effects on gene expression and/or splicing. They also form the basis for the investigation of the possible genetic role of MAPT in Parkinson's disease and other tauopathies, including Alzheimer's disease.