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Article

The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.

European journal of neurology - 1 May 2010

Damme P Van, Goris A, Race V, Hersmus N, Dubois B, Bosch L Van Den, Matthijs G, Robberecht W

Abstract excerpt

BACKGROUND AND PURPOSE: Mutations in fused in sarcoma (FUS) were recently identified as a cause of familial amyotrophic lateral sclerosis (ALS). The frequency of occurrence of mutations in FUS in sets of patients with familial ALS remains to be established. METHODS: We sequenced the FUS gene in a cohort of patients with familial ALS seen at the neuromuscular clinic in Leuven. A total of 28 patients with...

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Source

Identifiers

PMID: 19922450
DOI: 10.1111/j.1468-1331.2009.02859.x

Genes

FUS
SOD1

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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