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Disrupted N-linked glycosylation as a disease mechanism in deficiency of ADA2.
Adenosine deaminase 2 as a biomarker of macrophage activation syndrome in systemic juvenile idiopathic arthritis.
Genotype and functional correlates of disease phenotype in deficiency of adenosine deaminase 2 (DADA2).
Analysis of peripheral blood ADA1 and ADA2 levels in children and adults. Response to: 'Total adenosine deaminase highly correlated with adenosine deaminase 2 activity in serum' by Gao et al.
Polyarteritis nodosa and deficiency of adenosine deaminase 2 - Shared genealogy, generations apart.