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

G303V tau mutation presenting with progressive supranuclear palsy–like features

22 Nov 2011

Abstract excerpt

Additional Supporting Information may be found in the online version of this article. 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.

Read the complete abstract on PubMed

Topics

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

Share to Cellular transport and secretion
Share to Parkinson's Disease Mechanisms and Treatments
Share to Protein Kinase Regulation and GTPase Signaling

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Identifiers

PMID: 22109955
DOI: 10.1002/mds.24060

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

G303V tau mutation presenting with progressive supranuclear palsy–like featuresPMID 22109955Read ↗

Intraventricular tumor presenting as progressive supranuclear palsy-like phenotype.Semantic proximity Read ↗

Evolving concepts in progressive supranuclear palsy and other 4-repeat tauopathiesSemantic proximity Read ↗

Clinical and neuropathological features of progressive supranuclear palsy in Leucine rich repeat kinase (LRRK2) G2019S mutation carriers.Semantic proximity Read ↗

Spinocerebellar Ataxia Type 27B can be Suspected Based on Clinical Phenotype: The Massachusetts General Hospital Ataxia Center ExperienceSemantic proximity Read ↗

Expanding the Phenotypic Variability of PMPCA-Related Ataxia.Semantic proximity Read ↗

Ataxia-telangiectasia: A review of movement disorders, clinical features, and genotype correlations.Semantic proximity Read ↗

Progressive supranuclear palsy-like phenotype caused by progranulin p.Thr272fs mutation.Semantic proximity Read ↗

Progressive Supranuclear Palsy: an Update.Semantic proximity Read ↗

Tau gene delN296 mutation, Parkinson's disease, and atypical supranuclear palsy.Semantic proximity Read ↗

Two brothers homozygous for the TTR V30M both presenting with a phenotype dominated by central nervous complications.Semantic proximity Read ↗

SCA 17 phenotype with intermediate triplet repeat number.Semantic proximity Read ↗

Tau protein mutation P364S in two sisters: clinical course and neuropathology with emphasis on new, composite neuronal tau inclusions.Semantic proximity Read ↗

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