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Article

[Clinical and pathological characteristics of FUS/TLS-associated amyotrophic lateral sclerosis (ALS)].

Rinsho shinkeigaku = Clinical neurology - 1 Nov 2010

Murayama Shigeo

Abstract excerpt

FUS/TLS is identified as the causative gene of ALS6. FUS/TLS shares a role in nuclear protein as RNA editing with TDP43, and aggregates in basophilic inclusions (BIs) in ALS6 as well as juvenile ALS with BIs. FUS/TLS is also associated with atypical frontotemporal lobar degeneration (aFTLD), neuronal intermediate inclusion body disease (NIBD) and basophilic inclusion body disease (BIBD). Thus, FUS/TLS as well as...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21921522
DOI: 10.5692/clinicalneurol.50.948

Genes

FUS

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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