The Turkish Journal of Pediatrics 2020 , Vol 62 , Num 2
A rare case of syndromic severe congenital neutropenia: JAGN1 mutation
Funda Erol Çipe 1 ,Çiğdem Aydoğmuş 1 ,Kübra Baskın 1 ,Gonca Keskindemirci 1-2 ,Wojciech Garncarz 3 ,Kaan Boztuğ 3
1 Department of Pediatric Allergy and Immunology, Kanuni Sultan Suleyman Training and Research Hospital, İstanbul
2 Department of Social Pediatrics, İstanbul University Institute of Child Health, İstanbul, Turkey
3 CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, and Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria
DOI : 10.24953/turkjped.2020.02.022 Keywords :
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