Novel NFKB2 Mutation in Early-Onset CVID

被引：0
|
作者：
Liu, Y. [1 ]
Hanson, S. [1 ]
Gurugama, P. [1 ]
Jones, A. [2 ]
Clark, B. [1 ]
Ibrahim, M. [1 ]
机构：
[1] Kings Coll Hosp London, Dept Immunol Med, London, England
[2] Great Ormond St Hosp Sick Children, Dept Immunol, London WC1N 3JH, England
来源：
JOURNAL OF CLINICAL IMMUNOLOGY | 2014年 / 34卷
关键词：
D O I：
暂无
中图分类号：
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号：
100102 ;
摘要：
ESID-0064
引用
收藏
页码：S429 / S430
页数：2
相关论文
共 50 条
  • [1] Novel NFKB2 Mutation in Early-Onset CVID
    Yiwen Liu
    Steven Hanson
    Padmalal Gurugama
    Alison Jones
    Barnaby Clark
    Mohammad A A Ibrahim
    Journal of Clinical Immunology, 2014, 34 : 686 - 690
  • [2] Novel NFKB2 Mutation in Early-Onset CVID
    Liu, Yiwen
    Hanson, Steven
    Gurugama, Padmalal
    Jones, Alison
    Clark, Barnaby
    Ibrahim, Mohammad A. A.
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (06) : 686 - 690
  • [3] Novel NFKB2 mutation associated with early-onset common variable immunodeficiency
    Liu, Y.
    Hanson, S.
    Gurugama, P.
    Jones, A.
    Clark, B.
    Ibrahim, M. A. A.
    IMMUNOLOGY, 2014, 143 : 172 - 172
  • [4] More severe than CVID: Combined immunodeficiency due to a novel NFKB2 mutation
    Bienias, Marc
    Gabrielyan, Anastasia
    Geberzahn, Linda
    Roesen-Wolff, Angela
    Huebner, Angela
    Jacobsen, Eva-Maria
    Toepfner, Nicole
    Fang, Mingyan
    Lee-Kirsch, Min Ae
    Roesler, Joachim
    Schuetz, Catharina
    PEDIATRIC ALLERGY AND IMMUNOLOGY, 2021, 32 (04) : 791 - 795
  • [5] NFKB2 Mutation in 2 Siblings with DAVID Syndrome and CVID with Variable Presentations
    Kwiatkowski, Veronica
    Thanaputkaiporn, Narin
    Poowuttikul, Pavadee
    JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2022, 149 (02) : AB27 - AB27
  • [6] Early onset CVID and hypereosinophilia with novel VUS NFKB2 mutation c.1993A>T (p.Thr665Ser)
    Chang, Yatyng
    Lairet, Stephania
    Urschel, Daniel
    Cardenas, Melissa
    Hernandez-Trujillo, Vivian
    Calderon, Jose
    JOURNAL OF CLINICAL IMMUNOLOGY, 2022, 42 (SUPPL 1) : S45 - S45
  • [7] Novel Heterozygous Mutation in NFKB2 Is Associated With Early Onset CVID and a Functional Defect in NK Cells Complicated by Disseminated CMV Infection and Severe Nephrotic Syndrome
    Aird, Alejandra
    Lagos, Macarena
    Vargas-Hernandez, Alexander
    Posey, Jennifer E.
    Coban-Akdemir, Zeynep
    Jhangiani, Shalini
    Mace, Emily M.
    Reyes, Anaid
    King, Alejandra
    Cavagnaro, Felipe
    Forbes, Lisa R.
    Chinn, Ivan K.
    Lupski, James R.
    Orange, Jordan S.
    Cecilia Poli, Maria
    FRONTIERS IN PEDIATRICS, 2019, 7
  • [8] Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation
    Andrew W. Lindsley
    Yaping Qian
    C. Alexander Valencia
    Kara Shah
    Kejian Zhang
    Amal Assa’ad
    Journal of Clinical Immunology, 2014, 34 : 910 - 915
  • [9] Combined Immune Deficiency in a Patient with a Novel NFKB2 Mutation
    Lindsley, Andrew W.
    Qian, Yaping
    Valencia, C. Alexander
    Shah, Kara
    Zhang, Kejian
    Assa'ad, Amal
    JOURNAL OF CLINICAL IMMUNOLOGY, 2014, 34 (08) : 910 - 915
  • [10] A novel NFKB2 mutation in a Chinese patient with DAVID syndrome
    Xiao, Bing
    Fang, Di
    Liu, Huili
    Wang, Lili
    Qiu, Wenjuan
    GENE, 2019, 687 : 319 - 322
12345