Long-term clinical profile of children with the low-penetrance R92Q mutation of the TNFRSF1A gene
Pelagatti MA, Meini A, Caorsi R, Cattalini M, Federici S, Zulian F, Calcagno G, Tommasini A, Bossi G, Gattorno M
Arthritis Rheum · 2011
Key Findings
- ●R92Q associated with milder disease in children vs structural mutations
- ●Higher rate of spontaneous resolution with R92Q
- ●Lower amyloidosis risk compared to structural mutations
Referenced in (1 disease)
Validation history
Full log →- passsource metadataJun 1, 2026, 04:40 PMby pubmed-api
Stored DOI was incorrect; corrected to the PubMed-registered DOI (verified to resolve to this article).
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ID: pmid-21225694DOI: 10.1002/art.30237PMID: 21225694