Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy.

Movement disorders : official journal of the Movement Disorder Society - 30 Apr 2007

Williams David R, Pittman Alan M, Revesz Tamas, Lees Andrew J, de Silva Rohan

Abstract excerpt

A number of different clinical syndromes have been associated with progressive supranuclear (PSP) tau pathology. Previous reports have suggested that atypical clinical phenotypes of PSP occur in familial disease, and might be associated with mutations of MAPT. We examined the association of PSP-susceptibility tau haplotypes in pathologically diagnosed PSP, separated according to initial clinical features into...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to DNA
Share to MAPT gene

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genetic Variation

Share to London

Share to Reference Values

Share to Supranuclear Palsy, Progressive

Share to tau Proteins

Share to White People

Source

Identifiers

PMID: 17274033
DOI: 10.1002/mds.21393

Genes

MAPT

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation at the tau locus and clinical syndromes associated with progressive supranuclear palsy.PMID 17274033Read ↗

Genetic bases of Progressive Supranuclear Palsy: the MAPT tau disease.Semantic proximity Read ↗

Genetics of Progressive Supranuclear PalsySemantic proximity Read ↗

Genetics of Progressive Supranuclear Palsy: A ReviewSemantic proximity Read ↗

The H1c haplotype at the MAPT locus is associated with Alzheimer's disease.Semantic proximity Read ↗

Pathological, clinical and genetic heterogeneity in progressive supranuclear palsySemantic proximity Read ↗

Genetic and Epigenetic Constructs of Progressive Supranuclear PalsySemantic proximity Read ↗

Association of the MAPT locus with Parkinson's disease.Semantic proximity Read ↗

An extended 5'-tau susceptibility haplotype in progressive supranuclear palsy.Semantic proximity Read ↗

Evidence for a role of the rare p.A152T variant in MAPT in increasing the risk for FTD-spectrum and Alzheimer's diseases.Semantic proximity Read ↗

Motor and non-motor features in progressive supranuclear palsy: the impact of microtubule associated protein tau haplotypes among a Tunisian cohort.Semantic proximity Read ↗

The PSP-associated MAPT H1 subhaplotype in Guadeloupean atypical parkinsonism.Semantic proximity Read ↗

Association of MAPT haplotype-tagging SNPs with sporadic Parkinson's disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.