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3. The efficacy and safety of systemic corticosteroids as first line treatment for granulomatous lymphocytic interstitial lung disease

4. A dominant activating RAC2 variant associated with immunodeficiency and pulmonary disease

5. Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions

6. Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations

10. Multi-Institutional Experience of HSCT for DOCK8 Deficiency

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