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HARVARD Citation
Yılmaz Karapınar, D. et al. (2019). 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. 66 (10), p. n/a. [Online].