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2. Diagnostic Modalities Based on Flow Cytometry for Chronic Granulomatous Disease: A Multicenter Study in a Well-Defined Cohort

3. Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

4. The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency

5. IgM+IgD+CD27+ B cells are markedly reduced in IRAK-4–, MyD88-, and TIRAP- but not UNC-93B–deficient patients

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