In addition, alternative tau splicing as noted above has a tendency to differ depending on pathological phenotype, such that tau accumulation in AD is a mixture of 3R and 4R tau, Pick disease tends to be 3R tau, corticobasal degeneration and progressive supranuclear palsy tends to be 4R tau, and so-called argyrophilic grain disease accumulates small inclusions comprised of 3R tau. This evidence concerns the gene MAPT and progressive supranuclear palsy.