Çipe, F. E., Aydoğmuş, Ç., Baskın, K., Keskindemirci, G., Garncarz, W., & Boztuğ, K. (2020). A rare case of syndromic severe congenital neutropenia: JAGN1 mutation. The Turkish Journal of Pediatrics, 62(2), 326-331. https://doi.org/10.24953/turkjped.2020.02.022