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- W4200456173 endingPage "3160" @default.
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- W4200456173 abstract "Abstract Discovery of the VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome demonstrates that somatic mutations in haematological precursor cells can cause adult-onset, complex inflammatory disease. Unlike germline mutations, somatic mutations occur throughout the lifespan, are restricted to specific tissue types, and may play a causal role in non-heritable rheumatological diseases, especially conditions that start in later life. Improvements in sequencing technology have enabled researchers and clinicians to detect somatic mutations in various tissue types, especially blood. Understanding the relationships between cell-specific acquired mutations and inflammation is likely to yield key insights into causal factors that underlie many rheumatological diseases. The objective of this review is to detail how somatic mutations are likely to be relevant to clinicians who care for patients with rheumatological diseases, with particular focus on the pathogenetic mechanisms of the VEXAS syndrome." @default.
- W4200456173 created "2021-12-31" @default.
- W4200456173 creator A5017671399 @default.
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- W4200456173 creator A5088519611 @default.
- W4200456173 creator A5091742265 @default.
- W4200456173 date "2021-12-09" @default.
- W4200456173 modified "2023-10-18" @default.
- W4200456173 title "Somatic mutations in rheumatological diseases: VEXAS syndrome and beyond" @default.
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