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NeMO mutations: a rare cause of monogenic Behçet-like disease.

Rheumatology (Oxford, England) - 2 Mar 2021

Baldini Letizia, Di Sabatino Fabiana, Bodrero Enrico, Dellepiane Marta, Covizzi Carlotta, La Selva Roberta, Montin Davide, Licciardi Francesco

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PMID: 32954429
DOI: 10.1093/rheumatology/keaa505

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

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NeMO mutations: a rare cause of monogenic Behçet-like disease.PMID 32954429Read ↗

OR9-001 - Exome sequencing in monogenic Behçet-like diseaseSemantic proximity Read ↗

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NEMO splice variant causes distinct autoinflammatory syndrome.Semantic proximity Read ↗

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Phenotypes in Behçet’s syndromeSemantic proximity Read ↗

Different phenotypes identified for Behçet syndrome.Semantic proximity Read ↗

Disseminated BCG Infectious Disease and Hyperferritinemia in a Patient With a Novel NEMO Mutation.Semantic proximity Read ↗

A Novel Mutation in IKBKG/NEMO Leads to Ectodermal Dysplasia with Severe Immunodeficiency (EDA-ID).Semantic proximity Read ↗

EDA-ID and IP, two faces of the same coin: how the same IKBKG/NEMO mutation affecting the NF-κB pathway can cause immunodeficiency and/or inflammation.Semantic proximity Read ↗

A novel NEMO gene mutation causing osteopetrosis, lymphoedema, hypohidrotic ectodermal dysplasia and immunodeficiency (OL-HED-ID).Semantic proximity Read ↗

New insights into the pathogenesis and therapy of Behçet's diseaseSemantic proximity Read ↗

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