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...

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Detalles Bibliográficos
Autores principales: Luo, Xianze, Liu, Qing, Zhou, Lina, Tang, Xuemei, Zhao, Xiaodong, Zhang, Zhiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Research
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

Internet

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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