Comment on

• Progranulin gene mutations associated with frontotemporal dementia and progressive non-fluent aphasia.

  Snowden JS, Pickering-Brown SM, Mackenzie IR, Richardson AM, Varma A, Neary D, Mann DM. Snowden JS, et al. Brain. 2006 Nov;129(Pt 11):3091-102. doi: 10.1093/brain/awl267. Epub 2006 Sep 26. Brain. 2006. PMID: 17003069
• Novel splicing mutation in the progranulin gene causing familial corticobasal syndrome.

  Masellis M, Momeni P, Meschino W, Heffner R Jr, Elder J, Sato C, Liang Y, St George-Hyslop P, Hardy J, Bilbao J, Black S, Rogaeva E. Masellis M, et al. Brain. 2006 Nov;129(Pt 11):3115-23. doi: 10.1093/brain/awl276. Epub 2006 Oct 9. Brain. 2006. PMID: 17030534
• Frontotemporal dementia and parkinsonism associated with the IVS1+1G->A mutation in progranulin: a clinicopathologic study.

  Boeve BF, Baker M, Dickson DW, Parisi JE, Giannini C, Josephs KA, Hutton M, Pickering-Brown SM, Rademakers R, Tang-Wai D, Jack CR Jr, Kantarci K, Shiung MM, Golde T, Smith GE, Geda YE, Knopman DS, Petersen RC. Boeve BF, et al. Brain. 2006 Nov;129(Pt 11):3103-14. doi: 10.1093/brain/awl268. Epub 2006 Oct 9. Brain. 2006. PMID: 17030535
• The neuropathology of frontotemporal lobar degeneration caused by mutations in the progranulin gene.

  Mackenzie IR, Baker M, Pickering-Brown S, Hsiung GY, Lindholm C, Dwosh E, Gass J, Cannon A, Rademakers R, Hutton M, Feldman HH. Mackenzie IR, et al. Brain. 2006 Nov;129(Pt 11):3081-90. doi: 10.1093/brain/awl271. Brain. 2006. PMID: 17071926
• Mutations in progranulin explain atypical phenotypes with variants in MAPT.

  Pickering-Brown SM, Baker M, Gass J, Boeve BF, Loy CT, Brooks WS, Mackenzie IR, Martins RN, Kwok JB, Halliday GM, Kril J, Schofield PR, Mann DM, Hutton M. Pickering-Brown SM, et al. Brain. 2006 Nov;129(Pt 11):3124-6. doi: 10.1093/brain/awl289. Brain. 2006. PMID: 17071927