1 Clinical phenotype of a Chinese patient with RIPK1 deficiency due to novel mutation
来源:GENES DIS( P 2352-4820 E 2352-3042 ) 发表时间: 2020/03
类型:期刊论文 为本人加分:850.921198
贡献度:单独第一作者
2 The clinical, immunological and genetic features of 12 Chinese patients with STAT3 mutations
来源:ALLERGY ASTHMA CL IM( P 1710-1492 E ) 发表时间: 2020/07
类型:期刊论文 为本人加分:457.518990
贡献度:单独第一作者
3 Effective and safe treatment of a novel IL2RA deficiency with rapamycin
来源:J ALLER CL IMM-PRACT( P 2213-2198 E 2213-2201 ) 发表时间: 2020/03
类型:期刊论文 为本人加分:10.455762
4 Novel Heterogeneous Mutation of TNFAIP3 in a Chinese Patient with Behcet-Like Phenotype and Persiste..
来源:J CLIN IMMUNOL( P 0271-9142 E 1573-2592 ) 发表时间: 2019/02
类型:期刊论文 为本人加分:7.799722
贡献度:参与作者
5 DOCK2 couples with LEF-1 to regulate B cell metabolism and memory response
来源:BIOCHEM BIOPH RES CO( P 0006-291X E 1090-2104 ) 发表时间: 2020/08
类型:期刊论文 为本人加分:2.337449
贡献度:参与作者