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Article

Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western Europe

25 Sept 2003

Abstract excerpt

The Supplementary Material referred to in this article can be found at http://www.mrw.interscience.wiley.com/suppmat/1059-7794/suppmat/2003/v22.html Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.

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Identifiers

PMID: 14517953
DOI: 10.1002/humu.10269

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Research trail→

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Tau (MAPT) mutation Arg406Trp presenting clinically with Alzheimer disease does not share a common founder in Western EuropePMID 14517953Read ↗

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Slowly progressive dementia caused by MAPT R406W mutations: longitudinal report on a new kindred and systematic review.Semantic proximity Read ↗

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Homozygous MAPT R406W mutation causing FTDP phenotype: A unique instance of a unique mutation.Semantic proximity Read ↗

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Alzheimer disease-like clinical phenotype in a family with FTDP-17 caused by a MAPT R406W mutation.Semantic proximity Read ↗

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