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Neonatal-onset multisystem inflammatory disease responsive to interleukin-1beta inhibition
A de novo nonsense mutation in the tyrosine kinase lyn in a patient with an early onset autoinflammatory phenotype.
An autoinflammatory disease with deficiency of the interleukin-1-receptor antagonist
Mutational analysis in neonatal-onset multisystem inflammatory disease: Comment on the articles by Frenkel et al and Saito et al
