(Q44601555)

4 December 2017

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

1 reference

Christine Van Broeckhoven

4 December 2017

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7

object named as

Van Broeckhoven C

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4 December 2017

Rademakers R

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4 December 2017

Dermaut B

2

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4 December 2017

Peeters K

3

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4 December 2017

Cruts M

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4 December 2017

Heutink P

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4 December 2017

Goate A

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4 December 2017

1 November 2003

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4 December 2017

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4 December 2017

22

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4 December 2017

5

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4 December 2017

409-411

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Early-onset, rapidly progressive familial tauopathy with R406W mutation.

4 December 2017

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Autosomal dominant dementia with widespread neurofibrillary tangles.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Phenotypic correlations in FTDP-17.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Tau filament formation and associative memory deficit in aged mice expressing mutant (R406W) human tau.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Phenotypic variation in hereditary frontotemporal dementia with tau mutations.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10269

7 January 2021

Identifiers

DOI

10.1002/HUMU.10269

1 reference

4 December 2017

1 reference