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

Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias

30 May 2018

Abstract excerpt

International audience

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis Research
Share to Genetic Neurodegenerative Diseases
Share to Prion Diseases and Protein Misfolding

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 29848387
DOI: 10.1186/s40478-018-0547-8

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementiasPMID 29848387Read ↗

ATXN2 intermediate repeat expansions influence the clinical phenotype in frontotemporal dementiaSemantic proximity Read ↗

ATXN-2 CAG repeat expansions are interrupted in ALS patientsSemantic proximity Read ↗

ATXN2 CAG repeat expansions increase the risk for Chinese patients with amyotrophic lateral sclerosisSemantic proximity Read ↗

Intermediate Repeat Expansion in ATXN2 Gene as a Risk Factor in ALS and FTD Spanish PopulationSemantic proximity Read ↗

Role for ATXN1, ATXN2, and HTT intermediate repeats in frontotemporal dementia and Alzheimer's disease.Semantic proximity Read ↗

Intermediate Repeat Expansion in the ATXN2 Gene as a Risk Factor in the ALS and FTD Spanish PopulationSemantic proximity Read ↗

Recent Advances in the Genetics of Ataxias: An Update on Novel Autosomal Dominant Repeat ExpansionsSemantic proximity Read ↗

Identification of expanded repeats in NOTCH2NLC in neurodegenerative dementiasSemantic proximity Read ↗

Ataxin-2 gene: a powerful modulator of neurological disordersSemantic proximity Read ↗

Unexpanded and intermediate CAG polymorphisms at the SCA2 locus (ATXN2) in the Cuban population: evidence about the origin of expanded SCA2 alleles.Semantic proximity Read ↗

Expanded CAG Repeats in ATXN1, ATXN2, ATXN3, and HTT in the 1000 Genomes Project.Semantic proximity Read ↗

Ataxin-2 polyQ expansions in FTLD-ALS spectrum disorders in Flanders-Belgian cohortsSemantic proximity Read ↗

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