Altered Functions of Neutrophils in Two Chinese Patients With Severe Congenital Neutropenia Type 4 Caused by G6PC3 Mutations

BACKGROUND: SCN4 is an autosomal recessive disease caused by mutations in the G6PC3 gene. The clinical, molecular, and immunological features; function of neutrophils; and prognosis of patients with SCN4 have not been fully elucidated. METHODS: Two Chinese pediatric patients with G6PC3 mutations wer...

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Detalles Bibliográficos
Autores principales: Dai, Rongxin, Lv, Ge, Li, Wenyan, Tang, Wenjing, Chen, Junjie, Liu, Qiao, Yang, Lu, Zhang, Min, Tian, Zhirui, Zhou, Lina, Yan, Xin, Wang, Yating, Ding, Yuan, An, Yunfei, Zhang, Zhiyong, Tang, Xuemei, Zhao, Xiaodong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Immunology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296982/
https://www.ncbi.nlm.nih.gov/pubmed/34305938
http://dx.doi.org/10.3389/fimmu.2021.699743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8296982/
https://www.ncbi.nlm.nih.gov/pubmed/34305938
http://dx.doi.org/10.3389/fimmu.2021.699743

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