Absence of NLRP3 somatic mutations and VEXAS-related UBA1 mutations in a large cohort of patients with Schnitzler syndrome

Allergy. 2022 Nov;77(11):3435-3436. doi: 10.1111/all.15411. Epub 2022 Jun 25.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cohort Studies
  • Humans
  • Mutation
  • NLR Family, Pyrin Domain-Containing 3 Protein / genetics
  • Schnitzler Syndrome* / diagnosis
  • Schnitzler Syndrome* / genetics

Substances

  • NLR Family, Pyrin Domain-Containing 3 Protein
  • UBA1 protein, human

Supplementary concepts

  • VEXAS syndrome