Clinicopathologic heterogeneity in frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP ‐17) due to microtubule‐associated protein tau (MAPT) p.P301L mutation, including a patient with globular glial tauopathy

ConclusionsThis clinicopathologic study shows inter‐ and intra‐familial clinicopathologic heterogeneity of FTDP‐17 due to MAPT p.P301L mutation, including GGT in one patient.

Source: Neuropathology and Applied Neurobiology - March 7, 2017 Category: Neurology Authors: P. Tacik, M. Sanchez ‐Contreras, M. DeTure, M. E. Murray, R. Rademakers, O. A. Ross, Z. K. Wszolek, J. E. Parisi, D. S. Knopman, R. C. Petersen, D. W. Dickson Tags: Original Article Source Type: research