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Two patients with ZAP-70 deficiency in China present with a different genetic, immunological, and clinical phenotype
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 mutation...
Autores principales: | Luo, Xianze, Liu, Qing, Zhou, Lina, Tang, Xuemei, Zhao, Xiaodong, Zhang, Zhiyong |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10131425/ https://www.ncbi.nlm.nih.gov/pubmed/37101133 http://dx.doi.org/10.1186/s12887-023-03975-6 |
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