Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation

Title
Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF NEUROLOGY
Volume 15, Issue 4, Pages 377-385
Publisher
Wiley
Online
2008-02-18
DOI
10.1111/j.1468-1331.2008.02069.x

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