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Article

An Israeli Arab patient with a de novo TNFRSF1A mutation causing tumor necrosis factor receptor-associated periodic syndrome.

Arthritis and rheumatism - 1 Jan 2002

Aganna Ebun, Zeharia Avraham, Hitman Graham A, Basel-Vanagaite Lina, Allotey Rebecca A, Booth David R, Hawkins Philip N, Thacker Catherine, Syndercombe-Court Denise, McDermott Michael F

Abstract excerpt

OBJECTIVE: To investigate genetic susceptibility to recurrent fevers, generalized severe myalgia, and migratory erythema in an Israeli Arab child with no family history of similar disease. METHODS: DNA sequencing of exons 1-6 of the TNFRSF1A gene (formerly TNFR1) was performed in the patient and his parents to determine the presence of the autosomal-dominant tumor necrosis factor receptor-associated periodic...

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Source

Identifiers

PMID: 11817598
DOI: 10.1002/1529-0131(200201)46:1<245::AID-ART10038>3.0.CO;2-6

Genes

MEFV

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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