A homozygote novel L451W mutation in CECR1 gene causes deficiency of adenosine deaminase 2 in a pediatric patient representing with chronic lymphoproliferation and cytopenia
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M. Yılmaz | I. Sasmaz | S. Balcı | F. Incecik | G. Leblebisatan | A. Bişgin | Rabia Miray Kisla Ekinci