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; Brain: A Journal Of Neurology, 2006, vol. 129, issue Pt 11, p 3124, ISSN 14602156. ISBN 14602156.

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