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Article

TREX1 mutations are not associated with sporadic inclusion body myositis.

European journal of neurology - 1 Aug 2010

Cox F M, Boon E M J, van der Lans C A C, Bakker E, Verschuuren J J G M, Badrising U A

Abstract excerpt

BACKGROUND: Sporadic inclusion body myositis (sIBM) is the most frequent acquired myopathy above the age of fifty. The exact mechanism causing this disease is not known, but immune-mediated features are prominent and are probably to play a role in its pathogenesis. TREX1 gene mutations are associ...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 20192983
DOI: 10.1111/j.1468-1331.2010.02964.x

Genes

TREX1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-20192983-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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