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Screening of the SOD1, FUS, TARDBP, ANG, and OPTN mutations in Korean patients with familial and sporadic ALS.

Neurobiology of aging - 1 May 2012

Kwon Min-Jung, Baek Wonki, Ki Chang-Seok, Kim Hyun Young, Koh Seong-Ho, Kim Jong-Won, Kim Seung Hyun

Abstract excerpt

About 5% of amyotrophic lateral sclerosis (ALS) cases are known to be familial (fALS) and mutations in SOD1 and other genes are found in more than 20% of fALS patients and in 2%-4% of apparently sporadic ALS (sALS) cases. However, there are few reports on the proportion of fALS and the frequency of mutations in Korean patients with ALS. We screened mutations in the SOD1, FUS, TARDBP, ANG, and OPTN genes in 258...

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Source

Identifiers

PMID: 22244934
DOI: 10.1016/j.neurobiolaging.2011.12.003

Genes

SOD1
FUS
ANG
OPTN
TARDBP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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