Cite
MLA Citation
J Van Montfrans et al.. “Phenotypic variability in patients with ADA2 deficiency due to identical homozygous R169Q mutations.” Pediatric rheumatology online journal, vol. 13, no. 1, 2015, pp. 1–2. http://access.bl.uk/ark:/81055/vdc_100080417303.0x00056a