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...

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Bibliographic Details
Main Authors: Xianze Luo, Qing Liu, Lina Zhou, Xuemei Tang, Xiaodong Zhao, Zhiyong Zhang
Format: Article
Language:English
Published: BMC 2023-04-01
Series:BMC Pediatrics
Subjects:
Online Access:https://doi.org/10.1186/s12887-023-03975-6