Cite
MLA Citation
Rabia Miray Kisla Ekinci et al.. “A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia.” Pediatric hematology and oncology, vol. 36, 2019, pp. 376–381. http://access.bl.uk/ark:/81055/vdc_100092540543.0x000043