Two patients with ZAP-70 deficiency in China present with a different genetic, immunological, and clinical phenotype
Abstract Zeta(ζ)-Chain Associated Protein Kinase 70 kDa (ZAP-70) deficiency is a rare autosomal recessive primary immunodeficiency disease. Little is known about this disease. In this study, we report two patients to extend the range of clinical phenotypes and immunophenotypes associated with ZAP-70...
Saved in:
Main Authors: | Xianze Luo (Author), Qing Liu (Author), Lina Zhou (Author), Xuemei Tang (Author), Xiaodong Zhao (Author), Zhiyong Zhang (Author) |
---|---|
Format: | Book |
Published: |
BMC,
2023-04-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Natural isoaspartyl protein modification of ZAP70 alters T cell responses in lupus
by: Mei-Ling Yang, et al.
Published: (2023) -
Salt and pepper staining patterns for LAT, ZAP-70 and MUM-1 in a vasculitic bullousallergic drug eruption
by: Abreu Velez Ana Maria, et al.
Published: (2011) -
Genetic evidence for predisposition to acute leukemias due to a missense mutation (p.Ser518Arg) in ZAP70 kinase: a case-control study
by: Khalil Khashei Varnamkhasti, et al.
Published: (2024) -
Proliferative index and expression of CD38, Zap-70, and CD25 in different lymphoid compartments of chronic lymphocytic leukemia patients
by: Olga Khoudoleeva, et al.
Published: (2011) -
Mechanism and target treatment of primary immunodeficiency diseases with systemic lupus erythematosus‐like phenotype
by: Shan Liu, et al.
Published: (2024)