Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis
Background This study aimed to investigate the prevalence of mutations in the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK in Chinese pediatric patients with EBV-HLH.
基金：
Capital Medical Development Foundation of Beijing [2007-2062]; Beijing Health Bureau [2009-3-42]
第一作者机构：[2]Capital Med Univ, Beijing Childrens Hosp, Dept Virol Lab, Beijing 100045, Peoples R China
通讯作者：
通讯机构：[1]Capital Med Univ, Beijing Childrens Hosp, Dept Infect, Beijing 100045, Peoples R China;
推荐引用方式(GB/T 7714)：
Huang Zhizhuo,Xu Junmei,Shen Yuelin,et al.Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis[J].PEDIATRIC BLOOD & CANCER.2012,58(3):410-414.doi:10.1002/pbc.23216.
APA：
Huang Zhizhuo,Xu Junmei,Shen Yuelin,Qin Qiang,Liu Chunyan...&Shen Kunling.(2012).Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis.PEDIATRIC BLOOD & CANCER,58,(3)
MLA：
Huang Zhizhuo,et al."Screening the PRF1, UNC13D, STX11, SH2D1A, XIAP, and ITK gene mutations in Chinese children with Epstein-Barr virus-associated hemophagocytic lymphohistiocytosis".PEDIATRIC BLOOD & CANCER 58..3(2012):410-414
