Background and Clinical Features of a Unique and Mysterious Autoinflammatory Disease, Schnitzler Syndrome

Műzes G, Sipos F

Int J Mol Sci · 2025

Grade Ccase reportn=1Unverified
DOI ↗

Key Findings

  • ●Novel MEFV gene variant
  • ●F2 gene variant

Referenced in (1 disease)

Schnitzler Syndrome

Validation history

Full log →

No validation events recorded yet. Source will be checked on the next kipine-source-validator run.

ID: doi-10-3390-ijms26020598DOI: 10.3390/ijms26020598