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Mutations in progranulin explain atypical phenotypes with variants in MAPT


Mutations in presenilin-1 (PSEN1) cause autosomal dominant Alzheimer's disease and mutations in MAPT cause the familial tauopathy Frontotemporal dementia linked to chromosome 17 (FTDP-17). However, there have been reports of mutations in PSEN1 and MAPT associated with cases of FTD with ubiquitin-positive tau-negative inclusion pathology. Here, we demonstrate that the MAPT variants are almost certainly rare benign polymorphisms as all of these cases harbour mutations in Progranulin (PGRN). Mutations in PGRN were recently shown to cause ubiquitin-positive FTDP-17.

Type Journal
ISBN 1460-2156 (Electronic)
Authors Pickering-Brown, S. M.;Baker, M.;Gass, J.;Boeve, B. F.;Loy, C. T.;Brooks, W. S.;Mackenzie, I. R.;Martins, R. N.;Kwok, J. B.;Halliday, G. M.;Kril, J.;Schofield, P. R.;Mann, D. M.;Hutton, M. :
Publisher Name BRAIN
Published Date 2006-01-01
Published Volume 129
Published Issue Pt 11
Published Pages 3124-6
Status Published in-print
URL link to publisher's version