They are neurofibrillary-like pathologies in cases with the M337V and R406W mutations, Pick body-like tau structures in cases with the G272V, S320F, K369I, and G389R mutations, and PSP/CBD-like glial-dominant tau pathologies in most cases with missense or intron mutations in exon10/intron10 [14, 34]. Here, MAPT is linked to supranuclear palsy, progressive, 1.