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

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

Neurobiology of aging - 1 Apr 2013

Jang Ja-Hyun, Kwon Min-Jung, Choi Won Jun, Oh Ki-Wook, Koh Seong-Ho, Ki Chang-Seok, Kim Seung Hyun

Abstract excerpt

The expansion of a noncoding hexanucleotide repeat (GGGGCC) in the chromosome 9 open reading frame (C9orf72) gene has been identified as the most common cause of familial and sporadic amyotrophic lateral sclerosis (ALS) in Caucasian populations. The role of the C9orf72 repeat expansion in Korean ALS patients, however, has not been reported. We therefore investigated the frequency of the C9orf72 repeat expansion...

Read the complete abstract on PubMed

Topics

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

Share to Amyotrophic Lateral Sclerosis
Share to C9orf72 Protein

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Repeat Expansion

Share to Genetic Markers

Share to Prevalence

Share to Proteins

Share to Republic of Korea

Share to Risk Factors

Source

Identifiers

PMID: 23088937
DOI: 10.1016/j.neurobiolaging.2012.09.004

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of the C9orf72 hexanucleotide repeat expansion in Korean patients with familial and sporadic amyotrophic lateral sclerosis.PMID 23088937Read ↗

C9orf72 repeat expansions are not detected in Chinese patients with familial ALSSemantic proximity Read ↗

A hexanucleotide repeat expansion in C9ORF72 causes familial and sporadic ALS in Taiwan.Semantic proximity Read ↗

Large C9orf72 repeat expansions are seen in Chinese patients with sporadic amyotrophic lateral sclerosis.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 ↗

C9orf72 hexanucleotide repeat expansions in Chinese sporadic amyotrophic lateral sclerosis.Semantic proximity Read ↗

High frequency of the expanded C9ORF72 hexanucleotide repeat in familial and sporadic Greek ALS patients.Semantic proximity Read ↗

C9orf72 hexanucleotide repeat expansions and Ataxin 2 intermediate length repeat expansions in Indian patients with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Analysis of C9orf72 repeat expansion in 563 Japanese patients with amyotrophic lateral sclerosis.Semantic proximity Read ↗

Analysis of C9orf72 repeat expansions in Georgian patients with ALSSemantic proximity Read ↗

Japanese amyotrophic lateral sclerosis patients with GGGGCC hexanucleotide repeat expansion in C9ORF72.Semantic proximity Read ↗

Lack of C9ORF72 coding mutations supports a gain of function for repeat expansions in amyotrophic lateral sclerosis.Semantic proximity Read ↗

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

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