Cite
MLA Citation
Deniz Yılmaz Karapınar et al.. “Homozygous c.130–131 ins A (pW44X) mutation in the HAX1 gene as the most common cause of congenital neutropenia in Turkey: Report from the Turkish Severe Congenital Neutropenia Registry.” Pediatric blood & cancer, vol. 66, no. 10, 2019, p. n/a. http://access.bl.uk/ark:/81055/vdc_100089696657.0x000013