We did not observe any influence of any of the MAPT haplotypes on the suggestive or nominally significant SNPs, that is, the results observed in the association analysis were independent from the MAPT haplotype status. 3.1.3 Analysis of candidate genetic markers We then verified the relevance of other genetic risk factors that have previously been associated with FTD and/or closely related forms of neurodegenerative disease ( Table 5 ).
← all excerpts
A genome-wide screening and SNPs-to-genes approach to identify novel genetic risk factors associated with frontotemporal dementia.
1
—
—