• Retiring the term FTDP-17 as MAPT mutations are genetic forms of sporadic frontotemporal tauopathies 

      Forrest, SL; Kril, JJ; Stevens, C; Kwok, JB; Hallupp, M; Kim, W; Huang, Y; McGinley, C; Werka, H; Kiernan, MC; Gotz, J; Spillantini, MG; Hodges, JR; Ittner, LM; Halliday, GM
      Published 2017-01-01
      See Josephs (doi:10.1093/brain/awx367) for a scientific commentary on this article.In many neurodegenerative disorders, familial forms have provided important insights into the pathogenesis of their corresponding sporadic ...
      Open Access