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

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden.

Amyotrophic lateral sclerosis & frontotemporal degeneration - 1 Jan 2013

Akimoto Chizuru, Forsgren Lars, Linder Jan, Birve Anna, Backlund Irene, Andersson Jörgen, Nilsson Ann-Charloth, Alstermark Helena, Andersen Peter M

Abstract excerpt

An intronic GGGGCC-hexanucleotide repeat expansion in C9ORF72 was recently identified as a major cause of amyotrophic lateral sclerosis and frontotemporal dementia. Some amyotrophic lateral sclerosis patients have signs of parkinsonism, and many parkinsonism patients develop dementia. In this study we examined if the hexanucleotide repeat expansion was present in parkinsonism patients, to clarify if there could...

Read the complete abstract on PubMed

Topics

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

Share to DNA Repeat Expansion
Share to Genetic Markers

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to C9orf72 Protein

Share to Linkage Disequilibrium

Share to Parkinson Disease

Share to Prevalence

Share to Proteins

Share to Sweden

Source

Identifiers

PMID: 22985429
DOI: 10.3109/17482968.2012.725415

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 3 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

No GGGGCC-hexanucleotide repeat expansion in C9ORF72 in parkinsonism patients in Sweden.PMID 22985429Read ↗

C9ORF72 repeat expansions in Chinese patients with Parkinson's disease and multiple system atrophy.Semantic proximity Read ↗

Screening for C9orf72 repeat expansions in parkinsonian syndromes.Semantic proximity Read ↗

Large C9orf72 repeat expansions are not a common cause of Parkinson's diseaseSemantic proximity Read ↗

C9ORF72 intermediate repeat copies are a significant risk factor for Parkinson disease.Semantic proximity Read ↗

C9orf72 and its Relevance in Parkinsonism and Movement Disorders: A Comprehensive Review of the LiteratureSemantic proximity Read ↗

Parkinson disease is not associated with C9ORF72 repeat expansions.Semantic proximity Read ↗

Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

C9ORF72 hexanucleotide repeat expansions are a frequent cause of Huntington disease phenocopies in the Greek population.Semantic proximity Read ↗

Frontotemporal dementia, Parkinsonism and lower motor neuron involvement in a patient with C9ORF72 expansion.Semantic proximity Read ↗

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study.Semantic proximity Read ↗

Analysis of C9orf72 repeat expansions in Georgian patients with Amyotrophic lateral sclerosis (ALS)Semantic proximity Read ↗

The analysis of C9orf72 repeat expansions in a large series of clinically and pathologically diagnosed cases with atypical parkinsonismSemantic proximity Read ↗

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