Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.
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Coppola G, et al. Among authors: geschwind dh, geschwind md.
Hum Mol Genet. 2012 Aug 1;21(15):3500-12. doi: 10.1093/hmg/dds161. Epub 2012 May 3.
Hum Mol Genet. 2012.
PMID: 22556362
Free PMC article.