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Article

NEMO mutation as a cause of familial occurrence of Behçet's disease in female patients.

Clinical genetics - 1 Dec 2010

Takada H, Nomura A, Ishimura M, Ichiyama M, Ohga S, Hara T

Abstract excerpt

Behçet's disease is a chronic, relapsing, multisystem inflammatory disease of unknown etiology. Nuclear factor κB (NF-κB) essential modulator (NEMO) that is required for the activation of NF-κB plays an important role in inflammation. To investigate the role of NEMO in the pathogenesis of Behçet's disease, we analyzed NEMO gene and its expression pattern in tissues in a family with Behçet's disease. We found a...

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Identifiers

PMID: 20412081
DOI: 10.1111/j.1399-0004.2010.01432.x

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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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