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For contributors- A novel
BTK gene mutation, c.82delC (p.Arg28 Alafs*5), in a Korean family with X-linked agammaglobulinemia - Jeongeun Lee, Minhee Rhee, Taek Ki Min et al.
- Clin Exp Pediatr. 2016;59(Suppl 1):S49-S52.
- A novel
PRF1 gene mutation in a fatal neonate case with type 2 familial hemophagocytic lymphohistiocytosis - Jae Yeon Kim, Jeong Hee Shin, Se In Sung et al.
- Clin Exp Pediatr. 2014;57(1):50-53.
- A case of Hyper-IgE syndrome with a mutation of the STAT3 gene
- Ji-man Kang, Jungmun Suh, Jihyun Kim et al.
- Clin Exp Pediatr. 2010;53(4):592-597.