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HARVARD Citation
Van Montfrans, J. et al. (2015). Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations. Pediatric rheumatology online journal. 13 (1), pp. 1-2. [Online].
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Van Montfrans, J. et al. (2015). Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations. Pediatric rheumatology online journal. 13 (1), pp. 1-2. [Online].